Abstract
Immunocompromised mouse strains expressing human transgenes are being increasingly used in biomedical research. The genetic modifications in these mice cause various cellular responses, resulting in histologic features unique to each strain. The NSG-SGM3 mouse strain is similar to the commonly used NSG (NOD
Keywords
Immunocompromised mice are commonly used in biomedical research, and the various combinations of genetic manipulations have led to an ever-increasing number of different strains being encountered by pathologists.
5,80
One such mouse strain developed specifically to facilitate better engraftment of human myeloid cells and regulatory T cells
11
is the NSG-SGM3 (NOD.Cg-
The 3 human cytokine transgenes were chosen for various reasons. Specifically, the SCF/KIT ligand binds to the KIT receptor (CD117) 87 and supports the engraftment and differentiation of myeloid populations. It is also important in mast cell and eosinophil development. It is the only one of the 3 human cytokines in NSG-SGM3 mice that binds to both mouse and human receptor orthologs. 16 Meanwhile, GM-CSF is another strong inducer of myeloid differentiation, 26 whereas IL-3 can stimulate the proliferation of hematopoietic stem cells (HSCs) and the development of megakaryocytes, in addition to promoting both mast cell and basophil differentiation. 61
The mice described in this report were either naïve, had been “humanized” by transplantation of human CD34+ HSCs, or had been used to establish models of human leukemia. These mice were humanized by inoculating 4-week-old sublethally irradiated mice with human CD34+ (hCD34+) umbilical cord blood (UCB) HSCs. 62,81 Multilineage hematopoiesis occurs within 12 weeks. Another common use of NSG-SGM3 mice exploits their enhanced ability to engraft different types of human myeloid leukemia, 6,8,97,104 including human leukemia cell lines and leukemia patient-derived xenografts (PDXs). A less common leukemia model involves the implantation of human CD34+ HSCs that have been genetically modified via viral transduction to express leukemia-initiating factors. 6,57,95
This study describes the development of 3 general categories of histopathologic features in naïve and humanized NSG-SGM3 mice and in NSG-SGM3 mice implanted with transduced hCD34+ HSCs or leukemia PDXs. These features are believed to be due to the expression of the 3 human transgenes for SCF, GM-CSF, and Il-3 on the NSG background. Briefly, these features are mast cell hyperplasia, eosinophil hyperplasia, and the development of lesions resembling those of secondary hemophagocytic lymphohistiocytosis/macrophage activation syndrome (HLH/MAS). The development of this secondary HLH/MAS-like disease in NSG-SGM3 mice is likely due to activation of macrophages by the 3 human cytokines, especially GM-CSF. Interestingly, the development of histiocytic proliferations has been previously reported in humanized NSG mice implanted with CD34+ HSCs, 42,58,83 and we also include in this article evidence that these same proliferations develop in NSG mice when implanted with transduced hCD34+ HSCs and leukemia PDXs. The reports in humanized NSG mice did not describe the presence of hemophagocytosis, but it does occur to a mild degree in a subset of humanized NSG mice with histiocytosis. 14 This article will provide the reader with a comparison of histiocytosis in NSG mice with the more frequently severe hemophagocytic lymphohistiocytosis that develops in NSG-SGM3 mice and provide a rationale for our hypothesis that the NSG strain background of the NSG-SGM3 mice is prone to the proliferation of histiocytes and a mild degree of hemophagocytosis and that the addition of the transgenes causes exuberant proliferation, activation, and phagocytosis resulting in the clinical syndrome of HLH/MAS-like disease.
In this article, the features of mast cell and eosinophil hyperplasia and secondary HLH/MAS-like disease are described in NSG-SGM3 and NRG-SGM3 mice associated with studies at 4 research institutions (St. Jude Children’s Research Hospital [St. Jude], the University of California at Davis [UC Davis] via The Jackson Laboratory, the University of Michigan [U Mich], and the University of Texas MD Anderson Cancer Center [MDA]). All the mice associated with these different models exhibited similar phenotypes. One reason that mice from 4 institutions were evaluated was to examine whether there was an environmental contribution to the observations described. Because we believe the pathology of secondary HLH/MAS-like disease is related to the histiocytosis that can develop in humanized NSG mice, evaluation of the development of histiocytosis in NSG mice having had received transduced hCD34+ HSCs and NSG mice implanted with a B-ALL PDX is included. And finally, because secondary HLH/MAS is known to be associated with infections by viruses and other microorganisms, all NSG-SGM3 mice were examined by in situ hybridization (ISH) for the presence of Epstein-Barr virus (EBV), cytomegalovirus (CMV), and
Materials and Methods
Mice and Experimental Models
Animal care at all facilities
Mice housed at all facilities were maintained under strict specific pathogen-free barrier practices using sterilized water, food, bedding, and cages and were handled using aseptic techniques including the use of laminar flow hoods, personal protective equipment, and hair coverings. Mice were housed in temperature and humidity controlled rooms that are maintained on a 12:12 hour light–dark cycle with 10 to 15 room air changes per hour. All animals had
NSG-SGM3 mice
Evaluation of 3 naïve, unmanipulated mice (one 5-month-old male, one 5-week old male, and one 5-week old female) was performed as part of the routine care and surveillance of a breeding colony of NOD.Cg-
Humanized NSG-SGM3 mice
Humanization of 14 NSG-SGM3 mice was performed at The Jackson Laboratory when the mice were 4 weeks of age. Mice were irradiated with 100 cGy and injected via tail vein with hCD34+ UCB HSCs. At the respective institutions, mice underwent no other experimental manipulation and were monitored daily. Between 11 and 38 weeks after their arrival animals were submitted for histopathologic evaluation upon exhibiting various clinical signs (Table 1). Mice housed at The Jackson Laboratory were submitted to the Comparative Pathology Laboratory at UC Davis, and the mice at U Mich and MDA were submitted to their respective comparative pathology laboratories.
Experimental Details of 24 Affected NSG-SGM3/NRG-SGM3 Mice.
Abbreviations: UC Davis, University of California at Davis; U Mich, University of Michigan; F, female; M, male; HSCs, hematopoietic stem cells; PDX, patient-derived xenograft; AEL, acute erythroid leukemia; AML, acute myeloid leukemia.
aNRG-SGM3 strain.
NSG-SGM3 mice implanted with transduced hCD34+ umbilical cord blood (UCB) HSCs
Three mice from the St. Jude colony were implanted with human CD34+ UCB cells that had been transduced with a lentiviral vector carrying the fusion gene TCF3-ZNF384, which was predicted to cause leukemia. 25 At 8 weeks of age, 2.5 × 104 GFP-sorted cells were injected intrafemorally into sublethally irradiated (225 cGy) mice that were monitored daily for signs of illness. Mice were submitted for pathology evaluation between 12 and 20 weeks posttransplant (Table 1).
NSG-SGM3 mice implanted with PDX samples of acute erythroid leukemia (AEL)
The 8 NSG-SGM3 mice from AEL PDX studies were also from the St. Jude colony. PDXs were obtained by bone marrow biopsy and stored as cryopreserved cell suspensions in the St. Jude Biorepository. PDX samples were thawed and directly injected into mice without having been cultured or passaged in any mice. Three separate PDX samples were implanted into these 8 mice. AEL PDX #1 was implanted into 4 mice, AEL #2 into 3 mice, and AEL#3 into one mouse. At 9 weeks of age, mice were irradiated (250 cGy) prior to transplantation with 1.5 to 2 million cells via tail vein injection. Mice were monitored daily for signs of illness and were submitted for pathology evaluation between 4 and 32 weeks posttransplant. 43 One mouse from each group developed the abnormalities described below and underwent full histopathologic evaluation, and details for these 3 mice are in Table 1.
NRG-SGM3 mice implanted with AML PDX samples
Sixteen NRG-SGM3 (NOD.Cg-
NSG mice
A total of 23 NSG (NOD.Cg-
NSG mice implanted with transduced hCD34+ UCB HSCs
A group of 5 mice were implanted as described for NSG-SGM3 mice receiving these cells. At 32 weeks postimplantation all mice were sacrificed with none having shown any clinical signs of illness. Those with lesions are detailed in Table 2.
Clinical Characteristics of NSG Mice With Histiocytosis.
Abbreviations: HSCs, hematopoietic stem cells; PDX, patient-derived xenograft; B-ALL, B-acute lymphoblastic leukemia.
a Not known.
NSG mice implanted with B-ALL PDX
A total of 18 mice from a B-ALL study were evaluated. This cohort represented 15 individual PDX samples, with 11 of the 15 samples implanted into one mouse only, 2 of the 15 samples were implanted into 2 mice each, and one of the 15 samples was implanted into 3 mice. PDXs were obtained and treated the same as the NSG-SGM3 AEL PDX described above. Fourteen of these 18 mice had been irradiated (250 cGy) prior to transplantation via tail vein injection between 8 and 12 weeks of age. Mice were monitored daily and euthanized and submitted for pathology evaluation when they showed clinical signs of illness, between 10 and 38 weeks posttransplant. Those with lesions are detailed in Table 2.
A summary of the number of mice analyzed for each of the above models is shown in Table 3.
Number of Mice Evaluated for Each Model and Strain.
Abbreviations: HSCs, hematopoietic stem cells; AEL, acute erythroid leukemia; PDX, patient-derived xenograft; AML, acute myeloid leukemia.
Hematology Data
Whole blood was collected from NSG-SGM3 mice 10 to 20 (Table 1). At all institutions, it was collected via intracardiac puncture while under anesthesia as a terminal procedure. Blood was collected into tubes containing EDTA anticoagulant (BD Microtainer, BD Diagnostics). Complete blood counts (CBC) at St. Jude were performed on a ForCyte Hematology Analyzer (Oxford Science, Inc), at U Mich on a Hemavet 950FS, and at MDA on an Advia 2120i.
Tissue Processing and Handling
After being euthanized, the tissues collected from each mouse varied. Supplemental Table 1 indicates within each model how many mice had each tissue available for evaluation. The spinal cord was collected from those mice exhibiting ataxia. Organs collected were fixed in 10% neutral-buffered formalin and bones were subsequently decalcified in 10% formic acid. Tissues were embedded in paraffin, sectioned at 4 μm, and stained with hematoxylin and eosin (HE), and unstained slides were used for histochemical stains, immunohistochemistry, and in situ hybridization.
Histochemistry and Immunohistochemistry
The Prussian blue assay for iron was performed on the liver of mice 1 to 9, 13 to 21, 25, and 29 as well as on the spleen of mice 1 to 9, 13, 14, 17, 25 to 27, 29, and 30 using an Artisan Iron Stain Kit (Agilent [Dako], catalog # AR158) in conjunction with an Artisan Link Pro automated slide-staining system (Agilent). Mast cells were identified by using a toluidine blue stain (Poly Scientific, catalog # S284) and in immunohistochemical (IHC) labeling for mast cell tryptase (MCT) in mice 3, 6, 12 to 15, and 20 and for c-Kit/CD117 (SCF) in mice 12 to 14. Cells were identified as human by IHC labeling for human nuclear mitotic apparatus protein (hNuMA1). Cells of eosinophilic lineage were identified by IHC to human-specific and mouse-specific major basic protein (hMBP and mMBP, respectively) in mouse 16. In NSG-SGM3 mice, lymphocyte and macrophage cell populations were labeled by IHC for hCD68, hCD163, CD3, hCD4, hCD8, PAX5, hCD45, and F4/80 in the liver of all mice, the spleen of mice 1 to 17, and the central nervous system (CNS) of mice 1 to 4, 8, and 9. Leukemia cells were labeled for GFP in mouse 16, GATA1 in mouse 20, and myeloperoxidase (MPO) in mice 21 to 24. In NSG mice, implanted cells were labeled for hCD45 in the spleen of mouse 27 and for hNuMA1 in the bone marrow and spleen of mice 25, 26, and 30, and in the liver of mice 27 to 29. The reactivity for each antibody to the human and mouse antigen was verified by the laboratory (St. Jude) using either internal or external controls. The sources of antibodies and technical details for IHC assays are provided in Table 4.
Immunohistochemistry Methods for Antibodies Used in the Study.
Abbreviations: MCT, mast cell tryptase; MBP, major basic protein; GFP, green fluorescent protein; MPO, myeloperoxidase.
a Species reactivity; H, human; M, murine; N/A, not applicable.
b Ventana DISCOVERY ULTRA automated stainer, Ventana Medical Systems, Inc, Tucson, AZ.
cHeat-induced epitope retrieval, Cell conditioning media 2, Ventana Medical Systems, Inc.
d DISCOVERY OmniMap anti-rabbit HRP (760-4311), DISCOVERY ChromoMap DAB kit (760-159); Counterstain Hematoxylin II (Roche, Indianapolis, IN, 790-2208) and Blueing reagent (Roche, 760-2037).
eHeat-induced epitope retrieval, Cell conditioning media 1, Ventana Medical Systems, Inc.
f IVIEW DAB Kit (760-091); Counterstain Hematoxylin II (Roche, Indianapolis, IN, 790-2208) and Blueing reagent (Roche, 760-2037).
g intelliPATH FLX, BioCare Medical, LLC, Pacheco, CA.
hEnzyme-induced epitope retrieval with Proteinase K, DAKO S3020.
i Rabbit anti-rat secondary antibody (Vector Labs, BA-4001), Rabbit-on-Rodent AP-Polymer (BioCare Medical, Concord, CA, RMR625H), and Fast Red chromogen kit (BioCare Medical, IPK5017G80); Counterstain hematoxylin (BioCare Medical, IPCS5006L).
j HIER with Decloaking Chamber NsGEN and Target Retrieval, pH 6.
k Biotinylated rabbit anti-rat IgG, mouse absorbed secondary antibody (Vector Labs, BA-4001); Lab Vision streptavidin peroxidase (Thermo Scientific, TS-125-HR); DAB chromogen kit (Thermo Scientific, TA-125-QHDX); Counterstain hematoxylin (BioCare Medical, IPCS5006L).
l RTU, ready to use.
m Leica BOND-MAX automated stainer, Leica Biosystems, Buffalo Grove, IL.
n HIER with Bond Epitope Retrieval Solution 2 (ER2).
o Bond Polymer Refine Detection (DS9800); Counterstain Hematoxylin Refine Kit (Leica Biosystems, DS9800).
p HIER with Bond Epitope Retrieval Solution 1 (ER1).
q DISCOVERY OmniMap anti-rabbit HRP (760-4311), DISCOVERY ChromoMap Purple kit (760-229); Counterstain Hematoxylin II (Roche, Indianapolis, IN, 790-2208) and Blueing reagent (Roche, 760-2037).
In Situ Hybridization
RNAscope ISH probes for
Results
Mast Cell Hyperplasia in NSG-SGM3 Mice
Mast cell hyperplasia developed in all NSG-SGM3 mice evaluated by the veterinary pathologists at the institutions included in this study, including all mice described in this report. A murine mast cell hyperplasia occurred in naïve NSG-SGM3 mice which were part of the St. Jude breeding colony, whereas a human mast cell hyperplasia occurred in humanized mice and in mice implanted with transduced hCD34+ cells or a leukemia PDX. Both murine and human mast cell hyperplasia occurred predominantly and to the highest degree in the pancreas, but mild human mast cell hyperplasia also occurred in the stomach, small intestine, lung, spleen, and heart (not shown). Naïve unmanipulated NSG-SGM3 mice presented with varying degrees of periductular pancreatic mast cell accumulation (Fig. 1a). The cells were large and had prominent cytoplasmic granules (Fig. 1a, inset). The nuclei of these cells were not labeled by immunohistochemical staining with hNuMA1, verifying their murine origin (Fig. 1b). Mice implanted with human CD34+ HSCs or a leukemia PDX developed varying degrees of pancreatic infiltrates of human mast cells (Fig. 2a). The human mast cells were smaller than the murine mast cells, had less prominent granules, and spread interstitially instead of forming periductular aggregates (Fig. 2a, inset). Positive nuclear labeling with the antibody to hNuMA1 confirmed their human origin (Fig. 2b). Their identity as mast cells was demonstrated by metachromatic staining of the cytoplasmic granules (Fig. 2c) and by positive immunohistochemical labeling for CD117/c-Kit (Fig. 3a) and mast cell tryptase (MCT; Fig. 3b). The mice implanted with a leukemia PDX occasionally contained both murine and human mast cells (Fig. 4a, b). Human mast cells were also present in much lower numbers in the lamina propria of the stomach and of the small and large intestine, along with occasional resident murine mast cells (not shown).
Eosinophil Hyperplasia in NSG-SGM3 Mice
The bone marrow of humanized mice, mice implanted with transduced human CD34+ cells, and mice implanted with a leukemia PDX often showed human eosinophil hyperplasia. In humanized mice, the bone marrow eosinophil precursors were in patchy aggregates (Fig. 5 and inset) that varied in number between mice and between bones (sternum, vertebrae, limbs). A similar pattern was seen in mice with transduced-hCD34–derived leukemia (Fig. 6 and inset) and both in AEL and AML leukemia PDXs (Figs. 7, 8). The eosinophil precursors labeled with hMPB (Fig. 9) and were negative for mMBP (inset).
Mast cell hyperplasia, pancreas, naïve mouse. (a) Large aggregates of mast cells surround the pancreatic ducts and adjacent islets. Inset: there is a high level of granulation in these cells. Hematoxylin and eosin (HE). (b) The absence of nuclear labeling with antibody to hNuMA1 indicates that the cells are of mouse origin. The cytoplasmic color is nonspecific staining due to mast cell granules.
Histiocytic Proliferation in NSG Mice
Previous reports have documented a histiocytic proliferation in NSG mice when implanted with hCD34+ HSCs, 42,58,83 and the current study found that it can also occur when mice are implanted with transduced hCD34+ HSCs or a B-ALL PDX. Of the 5 NSG mice implanted with transduced hCD34+ HSCs, 2 mice developed large nodules of mature histiocytic cells, including multinucleated giant cells, in the spleen (Fig. 10), bone marrow (Fig. 11), and liver, with one of these two showing mild hemophagocytosis and iron accumulation in the splenic red pulp but not in the liver (Table 2). Histiocytic nodules developed in the same tissues in 4 of the 18 mice receiving a B-ALL PDX. These 4 mice were among those which had been irradiated prior to transplantation. The histiocytes in the liver nodules (Fig. 12a) were positive for hNuMA1 (Fig. 12b inset) indicating their human origin. The histiocytes were positive for hCD68 (Fig. 12c) and hCD163 (Fig. 12d) and were surrounded by mouse F4/80-positive macrophages (Fig. 12e). There was no evidence of hemophagocytosis or iron accumulation in 2 of the 4 mice (Fig. 12f), while it was present to a mild degree in the other 2 of the 4 mice (Table 2). The histiocytes were mixed with a few small hCD45+ (Fig. 12g) and CD3+ human lymphocytes (Fig. 12h).
Histiocytosis, spleen (Fig. 10) and bone marrow (Fig. 11), NSG mouse implanted with transduced hCD34+ cells (mouse 25). Hematoxylin–eosin (HE).
Secondary Hemophagocytic Lymphohistiocytosis/Macrophage Activation Syndrome (HLH/MAS)–Like Disease in NSG-SGM3 Mice, General Features
NSG-SGM3 mice developed a secondary HLH/MAS-like disease after undergoing humanization or implantation with transduced hCD34+ HSCs or a leukemia PDX. Morphologically, this disease is somewhat similar to the histiocytosis present in NSG mice, but with a much more activated phenotype as described below. It occurred in approximately 30% of humanized NSG-SGM3 mice (authors’ observations). The experimental details and clinical signs present in the study mice with this disease are detailed in Table 1. Typical clinical signs included hunched posture, lethargy, and pallor. Unlike in NSG mice with histiocytosis, anemia was a significant component of the HLH/MAS-like disease in NSG-SGM3 mice and was also the most likely cause of clinical illness prompting the removal of mice from a study. Markedly low hematocrit values were common, and the red blood cell parameters indicated a regenerative, macrocytic hypochromic type of anemia. Because a CBC was not performed for all mice, representative CBC data are shown for 3 mice: a humanized mouse, a mouse implanted with transduced hCD34+ cells, and a mouse implanted with a leukemia PDX (Table 5). Occasional mice had false indices of hyperchromasia, as shown in Table 5 for the mouse with transduced hCD34+ HSCs.
CBC Values in NSG-SGM3 Mice. Representative Examples for Humanized Mice, Mice Implanted With Transduced hCD34+ Cells, and Mice Implanted With an AEL PDX, Compared to Typical Values for Naïve NSG-SGM3 Mice.
Abbreviations: CBC, complete blood count; AEL, acute erythroid leukemia; PDX, patient-derived xenograft; HSCs, hematopoietic stem cells; HCT, hematocrit; RBC, red blood cells; HB, hemoglobin; MCV, mean corpuscular volume; MCH, mean cell hemoglobin; MCHC, mean cell hemoglobin concentration; RETIC, reticulocyte; N/D, not done.
a CBC values for 3 naïve NSG-SGM3 mice, showing range and mean.
b Mouse 12.
c Mouse 16.
d Mouse 20.
The histopathologic abnormalities seen in NSG-SGM3 mice with secondary HLH/MAS-like disease are detailed below for each individual model, but many features were common between all. In general, infiltrates of histiocytes with fewer lymphocytes were present predominantly in the spleen and liver, with less frequent and less severe infiltrates in lungs and bone marrow. An important and striking feature of these infiltrates was the marked enlargement of the histiocytes due to accumulation of intracytoplasmic iron and erythrocytes, consistent with hemophagocytosis. The degree of infiltration and organ distribution varied between organs and between the models evaluated as detailed below.
Secondary HLH/MAS-like disease in humanized SGM-SGM3 mice
The livers of humanized mice contained sinusoidal, perivascular, and portal infiltrates of histiocytes and lymphocytes. The sinusoidal infiltrates were more extensive than the perivascular or portal infiltrates, and occasionally the infiltrates were so severe that they replaced the liver parenchyma and accounted for most of the cells present in the liver (Fig. 13). However, the infiltrates were usually of only moderate severity (Fig. 14a). A large proportion of the inflammatory infiltrates consisted of medium to large macrophages, including multinucleated giant cells of human origin (Fig. 14b and inset), and these cells often contained cytoplasmic Prussian blue positive iron pigment (Fig. 14c). These macrophages expressed hCD68 (Fig. 14d) and hCD163 (Fig. 14e), and the cells were rimmed by mouse macrophages expressing F4/80 (Fig. 14f). The inflammatory infiltrates (Fig. 14g, HE) also consisted of CD3+ T cells (Fig. 14h) and PAX5+ B cells (Fig. 14i), with T cells generally being more numerous than B cells. Most of the T cells were CD4+ cells (Fig. 14j), but low numbers of CD8+ cells were also present (Fig. 14k).
Macrophage and lymphocyte infiltrates, liver, humanized NSG-SGM3 mice.
The spleens of humanized mice (Fig. 15a) had a similar composition of cellular infiltrates. The splenic red pulp was variably replaced by nodules or sheets of hNuMA1+ human macrophages (Fig. 15b), some of which had intracellular intact erythrocytes consistent with erythrophagocytosis (Fig. 15c) and many had abundant cytoplasmic iron (Fig. 15d). The splenic macrophages were similar to those in the liver but tended to include more hCD68+ than hCD163+ macrophages (Fig. 15e and f, respectively). The splenic white pulp was expanded with human lymphocytes (Fig. 15g) comprising variable proportions of CD3+ T cells (Fig. 15h) and PAX5+ B cells (Fig. 15i). The T cells were a mixture of hCD4+ and hCD8+ cells (Fig. 15j and k, respectively), with the former being dominant. Perivascular lymphohistiocytic infiltrates in the lungs were generally of minimal to mild severity and occasionally the histiocytes contained intracytoplasmic iron pigment (Fig. 16). The bone marrow contained variable patchy to scattered infiltrates of large macrophages and multinucleated giant cells (Fig. 17a). These cells occasionally contained intracytoplasmic iron pigment (Fig. 17a, inset) and were positive for hCD68 (Fig. 17b).
Histiocytosis, hemophagocytosis, and human lymphocyte engraftment; humanized NSG-SGM3 mouse (mouse 2).
Secondary HLH/MAS-Like Disease in Leukemia Bearing NSG-SGM3 Mice Implanted with Transduced Human CD34+ HSCs
The mice implanted with transduced human CD34+ HSCs developed a human myelomonocytic leukemia in the liver and bone marrow (Fig. 18a) that consisted of small cells (Fig. 18b) that were positive for myeloperoxidase (MPO; Fig. 18c) and hCD68 (Fig. 18d). The livers of these mice showed the same histiocyte accumulation with erythrophagocytosis that was seen in the livers of the humanized mice. Histiocyte aggregates were predominately sinusoidal, with fewer located in portal tracts and around the central veins. They were admixed with moderate numbers of lymphocytes (Fig. 19a). The macrophages often contained cytoplasmic pigment (Fig. 19a) and occasional intact intracytoplasmic erythrocytes (Fig. 19b). Both the macrophages and lymphocytes were of human origin, indicated by positive labeling for hNuMA1 (Fig. 19c). The pigment in the macrophages was identified as iron by Prussian blue staining (Fig. 19d). The macrophages were a mixture of hCD68+ and hCD163+ cells (Fig. 19e and f, respectively) surrounded by F4/80+ mouse macrophages (Fig. 19g). The transduced leukemia gene had been linked with a GFP reporter, and positively labeled leukemia cell aggregates were apparent (purple chromogen), whereas the large histiocytic cells were negative for GFP (Fig. 19h). These mice had fewer lymphocytes in the liver when compared to the humanized mice, but the lymphocytes that were present were a similar mixture of CD3+ T cells (Fig. 19i) and PAX5+ B cells (Fig. 19j).
NSG-SGM3 mice implanted with transduced hCD34-positive cells.
The overall cellular composition of the spleen (Fig. 20a) differed from that seen in humanized mice. The white pulp (Fig. 20a, b) was similarly populated by human CD3+ T cells (Fig. 20c) and PAX5+ B cells (Fig. 20d). However, the red pulp (Fig 20a, b) differed significantly from that of the humanized mice in that it was expanded by extramedullary hematopoiesis (EMH) and contained mild to moderate infiltrates of small histiocytes, with a notable absence of large multinucleated giant cells containing cytoplasmic pigment. The small histiocytes differed from those present in the spleens of humanized mice as they were positive for only hCD68 (Fig. 20e) and negative for hCD163 (Fig. 20f).
Engraftment of human leukemic cells and human lymphocytes, spleen, mouse implanted with transduced hCD34+ cells (mouse 17). (a) White starred areas indicate white pulp areas, black stars indicate red pulp. (b) The white pulp is populated by small lymphoid cells and the red pulp contains myeloid cells and extramedullary hematopoiesis. Hematoxylin-eosin (HE). (c–f) The white pulp contains a mixture of CD3-positive T cells (c) and PAX5-positive B cells (d). The myeloid cells in the red pulp are positive for hCD68 (e) and negative for hCD163 (f).
Secondary HLH/MAS-like disease in NSG-SGM3 mice after AEL PDX implantation
Of the 8 mice evaluated, 3 mice developed lesions that were further characterized by IHC and histochemistry for the present study. These 3 mice represented one mouse per group from each of the 3 AEL PDX samples, one of which had engrafted successfully and two of which had not. The leukemia PDX that engrafted replaced the bone marrow (Fig. 21a) and was positive for nuclear expression of GATA1 56 (Fig. 21b). Scattered among the leukemia cells in the bone marrow are macrophages containing iron pigment. Surprisingly, the liver had aggregates of human cells (Fig. 22a) that resembled those in humanized mice and in leukemia-bearing mice that had been implanted with transduced human CD34+ cells. The large, multinucleated macrophages had cytoplasmic pigment and occasional intracytoplasmic intact erythrocytes (Fig. 22b). The pigment was confirmed to be iron (Fig. 22c). The macrophages were positive for hCD68 and hCD163 (Fig. 22d and e, respectively) and were rimmed by F4/80+ mouse macrophages (Fig. 22f). They were admixed with low numbers of hNuMA1+ GATA1+ leukemia cells (Fig. 22g). Notably, there were no CD3+ T cells (Fig. 22h) nor any PAX5+ B cells present. In the 2 mice that did not engraft leukemia cells, the liver contained a few macrophage aggregates (Fig. 23a) with cytoplasmic pigment that was positive for iron by Prussian blue staining (Fig. 23b) and occasional CD3+ T cells (Fig. 23c) with no associated PAX5+ B cells. The bone marrow contained low to moderate numbers of macrophages containing iron pigment. Unfortunately, the spleens from these 3 mice were not available for histopathologic evaluation.
NSG-SGM3 mice implanted with acute erythroid leukemia (AEL) patient-derived xenografts (PDX).
Secondary HLH/MAS-like disease in NRG-SGM3 mice after AML PDX implantation
Sixteen mice from an AML PDX study were evaluated at the experimental endpoint of 20 weeks. Of these, 4 exhibited liver histiocytosis with erythrophagocytosis. The leukemia PDX was a myelomonocytic leukemia (Fig. 24) that expressed hCD163, hCD68, and MPO (not shown). However, the liver contained aggregates of cells that did not resemble the leukemia cells but were morphologically macrophages (Fig. 25a) of human origin, as confirmed by positive staining for hNuMA1 (Fig. 25b). The cells showed active erythrophagocytosis (Fig. 25c) and contained cytoplasmic pigment that was positive for iron by Prussian blue staining (Fig. 25d). They were positive for hCD68 and hCD163 (Fig. 25e and f, respectively) but only occasional cells expressed MPO (Fig. 25g). These aggregates had no associated CD3+ T cells (Fig. 25h) or PAX5+ B cells.
NRG-SGM3 mice implanted with an acute myeloid leukemia (AML) patient-derived xenograft.
Central nervous system histiocytosis in a subset of humanized NSG-SGM3 mice with HLH/MAS-like disease
An interesting phenomenon occurred in a subset of humanized NSG-SGM3 mice with HLH/MAS-like disease that was not seen in the leukemia-bearing mice given transduced hCD34+ HSCs or leukemia PDXs, nor has it been reported in humanized NSG mice to the authors’ knowledge. Affected mice developed an accumulation of mixed inflammatory cells in the meninges and an infiltration of macrophages into the CNS neuropil, predominantly within the cerebellum and regions of the spinal cord. They presented clinically with ataxia, head tilt, and/or hind limb paralysis (Table 1). The cerebellar and spinal cord meninges were thickened (Fig. 26a) with patches of human eosinophils (Fig. 26b), CD3+ T cells (Fig. 26c), and hCD68+ (Fig. 26d) and hCD163+ macrophages. There were also multiple foci of histiocytic cell infiltrates within the neuropil of the spinal cord and cerebellum (Fig. 27a). These cells were large, with abundant cytoplasm; however, in contrast to the cells in the liver and spleen, they had no cytoplasmic pigment and multinucleated giant cells were infrequent (Fig. 27b). The destructive mass effect of the histiocytic infiltrate was sometimes so severe as to suggest a neoplasm, as shown in Figure 27a and highlighted by immunohistochemical staining for hCD68 in Figure 27c. In the areas of neuropil infiltrates, only small numbers of lymphocytes were present along the border of the sheets of macrophages (Fig. 27d). Mouse F4/80-positive macrophages were also increased along the border (Fig. 27e).
Inflammatory cell infiltration of the CNS, humanized SGM-SGM3 mice.
Evaluation for EBV, CMV, and Mycoplasma
Because the presence of infectious agents is associated with the development of secondary HLH/MAS, all samples were analyzed for the presence of 3 pathogens by ISH. All of the tested samples (detailed in methods) were determined to be negative.
Discussion
A summary of the histopathologic features of the NSG-SGM3 mice described in this report and a comparison with what is observed in NSG mice are provided in Table 6. All of the lesions observed in the NSG-SGM3 mice in this study developed because human cells with the ability to differentiate into mast cells, eosinophils, and macrophages were implanted into the mice. For the humanized mice, this source was the implanted hCD34+ HSCs. In the case of the leukemia model created by injecting transduced hCD34+ HSCs, the source of cells comprising the lesions was probably nontransduced hCD34+ HSCs that were implanted along with the transduced leukemia progenitor cells. This is supported by the fact that the large human macrophages in the liver were negative for the GFP reporter. The nontransduced cells were likely a very small contaminating population as the cells had been GFP-sorted prior to implantation. The cell of origin in the leukemia PDX models is presumably a stem/progenitor population introduced with the PDX leukemia cells. This theory is supported by the observation of one of the authors (LJJ, unpublished data) that these lesions do not occur in NSG-SGM3 mice implanted with leukemia cell lines, suggesting that there is a contributing population within the PDX other than the neoplastic cells. The complex cellular environment of a PDX has both positive and negative consequences. PDX models are often employed when one is unable to develop a tumor cell line from a patient-derived sample, in which case the leukemia is established in immunocompromised mice. It is assumed that the additional cell types that are present provide supportive factors that enable PDX samples to proliferate in mice, and this cellular heterogeneity is one of the features that makes them more attractive than using tumor cell lines. 21,82,96 PDXs contain numerous cell types in addition to neoplastic cells, including stromal cells, blood vessel cells, immune cells, and, importantly, hematopoietic progenitors. However, these additional cellular factors might contribute to the negative consequences sometimes seen as a result of PDX implantation, and likely to the development of the secondary HLH/MAS-like disease described in this article. Other negative consequences have been demonstrated in the numerous reports of posttransplant lymphoproliferative disorders (PTLD) in NSG mice implanted with solid tumors 20,31,69,88,103 and of posttransplant graft-versus-host disease (GvHD). 77 PTLD generally involves the development of multisystemic lymphoplasmacytic infiltrates containing predominantly T cells with fewer B cells and/or B cell lymphoma. 50,64,88 GvHD is characterized largely by T cell infiltrates with damage to the epithelia of the skin, lung, liver, and gastrointestinal tract. 29,33 The inflammatory cell infiltrates in both PTLD and GvHD are of human origin and are believed to be derived from the xenograft. Notably, no abnormalities were present in the skin and gastrointestinal tract of the NSG-SGM3 mice in this study, and the lesions present in the lungs and liver did not include damage to epithelia. Furthermore, an important distinction between PTLD and GvHD and the inflammatory cell proliferations reported here in NSG-SGM3 mice is the predominance of myeloid-derived cellular proliferations (mast cells, eosinophils, and macrophages) in NSG-SGM3 mice. The following discussion will separately address the 3 categories of immune cell proliferations described in this report.
Summary of Models and Histopathologic Features Present.
Abbreviations: HLH/MAS, hemophagocytic lymphohistiocytosis/macrophage activation syndrome; CNS, central nervous system; HSC, hematopoietic stem cell; PDX, patient-derived xenograft.
a Historical controls.
b As reported in Henter et al. 39
c Described in current article.
d M, murine cells.
e H, human cells.
Mastocytosis
Given that SCF and IL-3 are important in mast cell development, it is not entirely unexpected that NSG-SGM3 mice can develop mast cell hyperplasia. The proliferation of mouse mast cells is the only abnormality regularly observed in naïve NSG-SGM3 mice, and it occurs because human SCF is cross-reactive and is, therefore, able to bind and activate murine SCF receptors. 16 The role of SCF in myeloid cell engraftment was studied by creating a mouse expressing membrane-bound human SCF (hSCF) on an NSG background. 87 After being humanized, these hSCF-NSG mice showed increased numbers of human mast cells when compared to humanized NSG mice without the transgenic hSCF, suggesting that this cytokine is sufficient for the proliferation of human mast cells. Unlike the situation in mice, in which recombinant murine IL-3 has been shown to be a strong inducer of mast cell proliferation, 63 human IL-3 does not by itself induce mast cell proliferation 51 but must be combined with other cytokines such as SCF 52 and/or interleukin 6 (IL-6) 76 to induce optimal mast cell proliferation. Previous studies using the NSG-SGM3 mouse have reported the presence of increased mast cells in various tissues such as the lung, spleen, stomach, small intestine, heart, and skin. 6,17 We similarly observed low numbers of human mast cells in all of these tissues except the skin. In the skin we observed moderate numbers of mast cells positive for MCT, but these were negative for hNuMA1, indicating that they were murine mast cells. The reason for the discrepancy between our findings and others is not clear but may be due to the antibody used to detect MCT. Although the antibody we used is labeled for human MCT, we observed in our own testing that it also labels mouse mast cells. Therefore, it is possible that the cells labeled in these previous publications were murine, as they were not verified to be human via hNuMA1 positivity or other such human-specific antigens. This is the first report of the presence of high numbers of human mast cells in the pancreas. It is possible that they were present in the mice examined in previous studies 6,17 but this specific tissue was not examined. It is unclear why the pancreas is a target organ for mast cells in these mice, as no clear role has yet been described for mast cells in either pancreatic homeostasis or pancreatic disease.
Eosinophil Hyperplasia
Eosinophil development and differentiation are dependent on essentially 3 cytokines: IL-3, GM-CSF, and interleukin 5 (IL-5). 32 In NSG-SGM3 mice, the excess production of both IL-3 and GM-CSF probably drives implanted HSCs toward eosinophil differentiation and hyperplasia. IL-3 and GM-CSF are necessary to promote the expansion of immature cells, which then commit to eosinophil/basophil differentiation upon the binding of IL-5. 32 Thus, the development of eosinophil hyperplasia in the NSG-SGM3 mouse is dependent upon the addition of IL-5. This could be provided by the implanted human cells or by the mouse itself, as murine and human IL-5 are cross-reactive. 59 The main source of IL-5 is CD4+/TH2 cells; 61 in humanized mice the IL-5 may be provided by the numerous engrafted human CD4+ T cells evident in the spleen and liver in the present study.
Secondary HLH/MAS-Like Disease
We have described the complex phenotype of the multisystemic accumulation of human macrophages, often accompanied by human lymphocytes, and the associated hemophagocytosis that occurs predominantly in the spleen and liver of NSG-SGM3 mice. This lesion occurred in a subset of humanized mice with no additional experimental manipulation between 11 and 38 weeks post humanization. A similar phenotype resulted when NSG-SGM3 mice were implanted with transduced hCD34+ HSCs or a leukemia PDX. The hemophagocytosis resulted in profound anemia, lethargy, overall poor health, and eventual morbidity requiring euthanasia. The macrophages were positive for hCD68 and hCD163, suggesting that these were more differentiated cells rather than immature macrophages, 27 with a tendency toward the M2 macrophage phenotype. 65 The macrophages had large accumulations of iron, and frank erythrophagocytosis was visible. These histopathologic findings, along with CBC data indicating a hemolytic anemia, suggest the mice have secondary HLH/MAS-like disease.
Our data enable a comparison between the appearance of histiocytic proliferation with occasional mild hemophagocytosis in NSG mice that have been humanized 42,58,83 or implanted with a PDX and the appearance and clinical manifestations of secondary HLH/MAS in similarly treated NSG-SGM3 mice. When describing histiocyte proliferations in humanized NSG mice that were not reported to be associated with hemophagocytosis, Huey et al used the diagnostic terms granulomatous inflammation and granulomatosis. 42 Given the proliferation of large epithelioid macrophages with multinucleated giant cells, this diagnosis is reasonable. In the current article, we have chosen to use the term histiocytosis because of the suspected connection with secondary HLH/MAS-like disease in NSG-SGM3 mice. It appears that the NSG strain background of the NSG-SGM3 mice is prone to the proliferation of histiocytes that sometimes exhibit hemophagocytosis, and the addition of the SGM3 transgenes (specifically GM-CSF as detailed below) causes exuberant proliferation, activation, and phagocytosis resulting in the clinical syndrome of HLH/MAS-like disease. Differentiating a hemophagocytic histiocytosis (such as that shown here in NSG-SGM3 mice) from other types of histiocytic proliferations (as shown in some NSG mice) is important both in animal models and in human diagnostics because other histiocytic disorders can show occasional hemophagocytosis cytologically and histologically. 72 Unfortunately there is no consensus on criteria for pathological hemophagocytosis versus occasional, incidental hemophagocytosis. 36,70 Key factors in establishing the diagnosis of a hemophagocytic disorder include the clinical appearance of anemia with or without other cytopenias, along with a high number of hemophagocytes. In humans, associated laboratory data are considered to be essential to making this diagnosis. 48 In the case of the NSG-SGM3 mice described in this article, the clinical features and very high number of hemophagocytes suggest they have true pathological hemophagocytosis. This delineation in the subset of NSG mice that show hemophagocytosis is less clear. In the 3 NSG mice implanted with transduced hCD34+ HSCs or a B-ALL PDX that had iron accumulation in the histiocytes, none had clinical signs suggesting anemia, but unfortunately blood for CBCs was not collected.
HLH/MAS is a syndrome of pathologic immune activation.
48
It is believed to result from lymphocytes activating macrophages, leading to excessive cytokine production and eventually a cytokine storm. In humans, HLH is characterized by fever, splenomegaly, cytopenias, increased triglycerides/decreased fibrinogen, and hemophagocytosis.
40
There are 2 types of HLH: genetic or familial (F-HLH) and secondary, of which the latter encompasses several subtypes. F-HLH was first described in 1952.
28
The first underlying genetic defect—mutations in the
A key factor in HLH/MAS is that it is the exaggerated immune response, culminating in a cytokine storm, that drives the disease pathology, not the underlying primary infection or another associated disorder. This dysregulated immune activation differs from many other immune disorders in that self-reactivity/autoimmunity is not the underlying mechanism.
48
Most of our current understanding of the pathophysiology of HLH is based on genetic animal models with defects in the
What is common to F-HLH and secondary HLH is that macrophages are central to disease development, and it is their activation and subsequent cytokine production that is key. However, in secondary HLH, CD8+ T cells may be sufficient upstream drivers of macrophage activation, although not necessary. The ability of macrophages by themselves to mediate the development of secondary HLH has been suggested by studies in which repeated TLR9 10 stimulation produced an HLH/MAS-like disease in mice; this was found to be dependent on IFN-γ but not on the presence of lymphocytes. 19 Recently, Akilesh and colleagues described the ability of chronic TLR7 and TLR9 signaling to stimulate the development of a type of macrophage they termed an “inflammatory hemophagocyte,” 4 suggesting a link between TLR signaling and the activation of macrophages leading to HLH/MAS-like disease.
The primary role of macrophages and the lesser role of lymphocytes in HLH/MAS pathogenesis has been demonstrated in several mouse studies. 15,99,100 The authors of one such study injected NSG-SGM3 mice with unfractionated UCB that had been depleted of T cells, which induced a syndrome that the authors identified as MAS and that resembled the secondary HLH/MAS-like disease described in the present study. 99 Of the mice so treated, 30% became moribund between 16 and 20 weeks of age, which is similar to the latency observed in the present study. Anemic, clinically ill mice treated with dexamethasone, immunoglobulin, or anti-B/T cell antibodies showed no improvement, whereas treatment with gemtuzumab ozogamicin, a CD33-targeting myeloablating drug, resulted in the reversal of anemia and a marked improvement in their clinical appearance. An analysis of serum cytokines from the UCB-engrafted mice showed a significant increase in IL-6 and small but insignificant increases in IFN-γ and tumor necrosis factor-α (TNF-α), which have been demonstrated to be key drivers in genetic models of HLH. 46,54,105 A separate study followed the development of posttransplant HLH in NSG-SGM3 mice humanized by a different method using hCD34+ fetal liver cells. 100 In that study, there was a similar latency period of 17 to 22 weeks, and histologic liver lesions resembled those described in the present report, with an accumulation of large multinucleated hCD68+ macrophages containing iron, and CD3+ T cells. Flow cytometry analysis of peripheral blood T-cell subsets showed an increased CD4:CD8 ratio, which is consistent with the findings in the present study. The serum levels of numerous cytokines, namely IFN-γ, TNF-α, IL-6, and GM-CSF, were elevated in the humanized NSG-SGM3 mice, as compared to the non-humanized NSG-SGM3 mice. 100 The finding of increased IL-6 in these 2 studies is consistent with what has been found in some human HLH/MAS studies. 22,71 However, IL-6 inhibition with tocilizumab (an anti-IL6R antibody) has not proved effective at treating the disease in humans. 35,78
Regarding the disease in NSG-SGM3 mice described in this report, overexpressed human GM-CSF is probably the key macrophage-activating cytokine driving secondary HLH/MAS-like disease. Briefly, this is because human studies and animal models of HLH/MAS have shown it to be a key cytokine in driving the disease, and because GM-CSF is a known potent activator of macrophages. This cytokine can act directly upon the implanted cells because the receptor for GM-CSF is expressed on human CD34+ hematopoietic progenitors. 79 GM-CSF is not essential for normal homeostasis, but it participates in the rapid expansion and differentiation of myeloid cells as part of an inflammatory response. 26 The exact function of GM-CSF in various disease conditions is complex, as it has been implicated in promoting numerous inflammatory diseases such as rheumatoid arthritis, multiple sclerosis, and some forms of colitis, whereas other studies have shown it to promote antitumor immunity and to participate in the resolution of inflammation during infection. 9,26,102 An extensive body of research has demonstrated the myriad roles of GM-CSF in hematopoiesis and inflammation. Relevant to the current study is the demonstration that GM-CSF induced HLH in a human patient receiving the cytokine along with chemotherapy for lymphoma. 73 Similarly, it was shown to exacerbate hemophagocytosis associated with myelodysplastic syndrome. 94 Reviews of GM-CSF are available. 9,26,38,90,102 Here we will discuss only selected studies that are directly relevant to the contribution of GM-CSF to the development of the HLH/MAS-like disease in NSG-SGM3 mice.
The most relevant role of GM-CSF in relation to the development of the secondary HLH/MAS-like disease in NSG-SGM3 mice is its effect on macrophages. In vitro studies have shown that when grown in culture in the presence of GM-CSF, mouse bone marrow will produce both macrophages (MHCIIlowF4/80high) and dendritic cells (MHCIIhighF4/80low) but that the proportion of macrophages increases with increasing doses of GM-CSF. 66 The types of macrophages that develop under the influence of GM-CSF are not clearly of the M1 or M2 type. 65 They produce higher levels of inflammatory cytokines, specifically TNF-α, IL-6, interleukin 12 p70 (IL-12p70), and interleukin 23 (IL-23), than do M-CSF (macrophage colony-stimulating factor)–derived macrophages 30 or GM-CSF–derived dendritic cells. 66 The transgenic expression of GM-CSF in NSG-SGM3 mice could well be at a sufficiently high level to drive the production of large numbers of macrophages expressing high amounts of inflammatory cytokines, thereby influencing the development of secondary HLH/MAS-like disease.
The in vivo role of GM-CSF has been investigated by inducing its overexpression in mice. 55 The most remarkable hematopoietic finding was the marked accumulation of peritoneal macrophages that were twice the size of the controls. Interestingly, these cells had enhanced Fc-dependent phagocytosis of antibody-coated sheep erythrocytes, 89 perhaps providing evidence that GM-CSF drives hemophagocytosis in secondary HLH/MAS-like disease. This model also showed prominent infiltration of macrophages into the eyes, primarily in the vitreous humor but also in the anterior and posterior chambers and subretinally. 55 Such eye lesions were not present in the mice examined in the present study.
Further research has examined the effects of the production of GM-CSF by specific cell types. When examined at 6 weeks of age, C57BL/6 mice with conditional overexpression of GM-CSF in their T cells showed partial effacement of the lymph nodes, spleen, and thymus by histiocyte-like cells, with occasional multinucleated giant cells. 92 The lung, kidney, and liver had varying degrees of granulocyte and histiocyte infiltration. Evaluation of the histiocyte-like cells by flow cytometry revealed them to be a mixture of monocytes, macrophages, and dendritic cells.
In the present study we found a proliferation of histiocytes in the CNS of some humanized NSG-SGM3 mice, which we have not seen, nor are we aware of being reported, in humanized NSG mice. Although we did not observe hemophagocytosis within these CNS lesions in the mice, CNS involvement does occur with HLH/MAS in humans. It is generally estimated that around one third of patients with HLH/MAS show CNS symptoms 41,45,48 but some studies have observed as high as 73%. 37 Diagnosis is generally made using MRI (magnetic resonance imaging) or CT (computed tomography) imaging. 18,34 Occasionally a brain biopsy is undertaken or the diagnosis is made at autopsy. Lesions in the brain range from mild histiocytic or lymphohistiocytic leptomeningeal infiltrates to diffuse infiltration of the neuropil with large numbers of CD68+ histiocytes and CD3+ T cells with fewer B cells. 39,49,53
We suspect that the activity of GM-CSF is implicated in the nervous system abnormalities. Interestingly, conditional expression of GM-CSF in the peripheral CD4+ T cells of C57BL/6 mice 84 resulted in neurologic defects (ataxia, circling) around 12 weeks after induction. Early in the process, this was associated with CNS-infiltrating myeloid cells (monocytes and neutrophils) but with a notable absence of T cells, whereas later in the disease course, T cells began to infiltrate as well. These cells often formed solid masses, particularly in the brain stem and, less abundantly, in the spinal cord, which was the same pattern observed in the mice in the present study. RNA sequencing showed the gene expression profile of inflammatory monocyte-derived cells in the CNS to be vastly different from that of similar cells in all other organs examined. 84 Further characterization of the histiocytic subsets that are composing these lesions in the NSG-SGM3 mice is needed to see if they represent a unique population.
An interesting question yet to be answered is why only some mice develop secondary HLH/MAS-like disease, and why a subset of those then go on to develop the CNS phenotype. Their development may be influenced by host factors and/or factors intrinsic to the implanted cells. We theorized that some hCD34+ HSCs and PDXs contain inactive microorganisms that are reactivated following introduction into the immunocompromised NSG-SGM3 mouse. The lesions were examined for the presence of EBV and CMV because of their association with HLH/MAS, 70,75 and for mycoplasma because of its propensity to contaminate cell products and affect experimental findings. 13,91,101 By ISH, these organisms were not detected in our samples, which suggests they are not the cause in this group of mice. Additional studies are necessary to determine the initiating factors, with the goal being to eliminate these factors and thus prevent the development of this confounding syndrome.
The results of our study indicate that when evaluating NSG-SGM3 mice that have been implanted with human cells, one must carefully confirm the cell population(s) generated. We demonstrated how this is important in the context of leukemia studies, but it is also relevant in other study types such as infectious disease studies. The complexity of cell populations is compounded in studies combining multiple types of implanted human cells, as is often done for immunotherapy. 21,23,86 Such studies have been conducted in NSG mice, including the use of anti-PD1 74,93 and CAR-T 2,47 cell therapy. These studies have shown humanized mice to be a superior model in testing immunotherapies, and it is likely that similar studies in NSG-SGM3 mice are currently being conducted. All three of the features described here could confound the results of studies using NSG-SGM3 mice. Because the proliferating human mast cells do not resemble typical mouse connective tissue mast cells, they may be mistaken for other cell types. Although eosinophils are not difficult to recognize in tissue sections, one might misinterpret their increased number as being completely due to the experimental manipulation instead of recognizing that the human transgenes could be affecting their numbers. Regarding the occurrence of secondary HLH/MAS-like disease, the use of survival or CBC data such as anemia as an endpoint must be accompanied by histopathologic evaluation in order to confirm the cause of death. This is particularly important in AML studies, in which anemia leading to lethargy and eventual euthanasia is a commonly used endpoint, 44,60 as the causes of the anemia could be confusing and difficult to differentiate.
It is possible that future studies will demonstrate that the disease seen in NSG-SGM3 mice, which we have termed secondary HLH/MAS-like disease, does in fact reflect the condition in humans and may serve as a model of HLH/MAS. As so many conditions are associated with the development of the syndrome in humans, the final manifestations are probably an endpoint associated with numerous pathways. In view of this, it is likely that no single model will be able to mimic the human condition completely, but perhaps the lesions described here will provide some insight into its mechanisms.
Supplemental Material
Supplemental Material, Combined_supplemental_materials-Janke_et_al - Development of Mast Cell and Eosinophil Hyperplasia and HLH/MAS-Like Disease in NSG-SGM3 Mice Receiving Human CD34+ Hematopoietic Stem Cells or Patient-Derived Leukemia Xenografts
Supplemental Material, Combined_supplemental_materials-Janke_et_al for Development of Mast Cell and Eosinophil Hyperplasia and HLH/MAS-Like Disease in NSG-SGM3 Mice Receiving Human CD34+ Hematopoietic Stem Cells or Patient-Derived Leukemia Xenografts by Laura J. Janke, Denise M. Imai, Heather Tillman, Rosalinda Doty, Mark J. Hoenerhoff, Jiajie J. Xu, Zachary T. Freeman, Portia Allen, Natalie Wall Fowlkes, Ilaria Iacobucci, Kirsten Dickerson, Charles G. Mullighan, Peter Vogel and Jerold E. Rehg in Veterinary Pathology
Footnotes
Acknowledgements
The authors thank the St. Jude Animal Resource Center and the Veterinary Pathology Core for technical assistance. The authors thank Keith A. Laycock, PhD, ELS, for scientific editing of the manuscript.
Declaration of Conflicting Interests
The author(s) declare no potential conflicts of interest with respect to the research, authorship, or publication of this article.
Funding
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This publication was supported, in part, by Grants R35CA197695-01A1 and CA021765 from the National Cancer Institute, the St. Jude Chromatin Collaborative, the Leukemia and Lymphoma Society Translational Research Program, and the American Lebanese Syrian Associated Charities (ALSAC). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
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