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Abstract

Corneal Langerhans cells (LCs) offer the opportunity to gain insight into the activity of the innate immunity. We examined the density and the distribution of LCs and compared the results with dry-eye parameters in rheumatoid arthritis (RA). Fifty-two RA patients with various degrees of disease activity and 24 healthy subjects were enrolled. Peripheral and central LC number and morphology were assessed with in vivo laser confocal microscopy. In addition, ocular surface disease index (OSDI), lid parallel conjunctival folds, Schirmer test, and tear break-up time (TBUT) were evaluated. The prevalence of central and peripheral LC, and the central LC morphology values (LCM) were higher than normal in RA. Within the RA group, LC prevalence and morphology were not affected by disease activity. However, patients on anti-TNF or glucocorticosteroid (GCS) therapy exhibited normal LCM, and normal central and peripheral LC density. OSDI was higher and TBUT was lower than normal in RA. The alteration of LC in RA suggests an active inflammatory process in the cornea, which may reflect an increased activation state of the innate immune system—even in inactive stages of RA and without ocular symptoms. The results also indicate ocular effects of GCS therapy in RA.

Keywords

Anti-TNF therapy corneal Langerhans cell rheumatoid arthritis

Introduction

Although the predominant feature of rheumatoid arthritis (RA) is joint involvement, further extra-articular manifestations, including ocular involvement, may also be present. The most common ocular problems in RA are sicca symptoms and about 10% of RA patients develop secondary Sjögren’s syndrome.¹ Episcleritis, scleritis and a variety of corneal changes, including keratitis and keratoconjunctivitis sicca, may also occur. The cells participating in these processes, however, are poorly clarified. The highly potent antigen-presenting dendritic cells, the so-called corneal Langerhans cells (LCs), act as potent inducers and regulators of local corneal immune processes.^2–4 They can stimulate both primary and secondary T- and B-cell responses. The distribution and role of LCs in the central cornea is an issue of ongoing discussion. Several investigators have demonstrated the presence of LCs in the epithelium and stroma of the central cornea ex vivo.^5–7 Moreover, the presence of LCs in the central corneal epithelium of healthy volunteers has also been documented.⁶ Detailed information concerning the maturation and migration of LCs in response to cytokines and chemokines is not yet fully available,^3,8,9 but some data suggest the principal role of pro-inflammatory cytokines, including TNF-α.^10,11 In recent years new techniques that directly visualize microscopic changes of ocular structures in vivo have become available for clinical use. Confocal microscopy, first described by Minsky,¹² now applies a laser beam to obtain coronal optical sections of the cornea and to collect data even on the prevalence of certain cell subtypes. With this new tool we characterized the presence and distribution of LCs in the corneal epithelium of RA patients with various disease severities.

Materials and methods

Patients

Fifty-two RA patients with variable severity and duration of disease, and 24 healthy individuals were enrolled (see clinical characteristics in Table 1). RA patients were classified according to the latest American College of Rheumatology/European League Against Rheumatism (ACR/EULAR criteria).¹³ Written informed consent was obtained from all subjects, and our study was reviewed and approved by an independent ethics committee of the institution. The study adhered to the tenets of the most recent revision of the Declaration of Helsinki. Disease activity score 28 (DAS28) was calculated at the time of the eye examination. All RA patients received at least one of the following disease-modifying anti-rheumatic drugs (DMARD): methotrexate (69%), leflunomide (17%), sulfasalazine (1%) and chloroquine (1%). Twenty-three of 52 RA patients (44%) received an anti-TNF agent, and 16 of 52 RA patients were also treated with low-dose oral glucocorticoids (GCS) and DMARD and/or anti-TNF agent together. At the time of evaluation of confocal microscopic investigation, none of the patients suffered any overt ocular symptom requiring specific ophthalmic assistance. Patients with diabetes; previous eye surgery; uveitis within one year prior to examination; glaucoma; congenital, mechanical or toxic injury of the cornea; or illnesses causing corneal edema, haze or scars were excluded. RA patients with secondary Sjögren’s syndrome diagnosed according to the revised version of the European criteria for Sjögren’s syndrome were omitted from the study.¹⁴ Patients with Schirmer test results of less than 5 mm/5 min were not excluded automatically from the study if the results of other functional tests and histology were normal, and no anti-Ro(SSA) or anti-La(SSB) Abs were detected.

Table 1.

Clinical characteristics of healthy individuals and RA patients. Data are expressed as median [interquartile range].

Characteristics	Healthy individuals n = 24	RA patients n = 52
Age (years)	61 [52.5–67]	58 [49–66]
Gender (male/female)	10/14	9/43
RA duration (years)	–	8 [3.75–15]
DAS28	–	2.30 [1.76–3.52]
No. of patients receiving anti-TNF-α therapy	–	23 (44.2%)
No. of patients receiving DMARD therapy		29 (55.8%)
No. of patients receiving glucocorticosteroid therapy		16 (30.8%)

Eye examinations

All examinations were carried out on the right eye only in the same room among unchanged conditions.

Dry eye examinations

An ocular surface disease index (OSDI) questionnaire was used to evaluate the subjective ocular discomfort.¹⁵

Lid parallel conjunctival folds (LIPCOF) are subclinical folds of the conjunctiva, situated at the temporal and nasal aspect of the bulbar conjunctiva. Loosened conjunctiva creating folds, detectable by slit lamp are thought to reflect dryness of the ocular surface. According to the height and morphology, grading can be made on a 0–3 scale reflecting the severity of dry eye. LIPCOF was measured at the temporal aspect of the lower eyelid margin during routine slit lamp examination, according to the protocol by Pult.¹⁶

The Schirmer-strip (Haag-Streit, UK, Ref: 4701001) was used to evaluate tear production and was placed at the temporal aspect of the lower conjunctival sac. Values were read after 5 min with the help of a ruler.

Tear break up time (TBUT) was determined after instillation of one drop of fluorescein dye into the lower conjunctival sac.

In vivo confocal microscopy investigations

All patients were examined with a digital corneal confocal laser-scanning microscope (HRT II RCM Heidelberg Engineering Inc., Heidelberg, Germany, Rostock Cornea Module), equipped with the in-built software Heidelberg Eye Explorer version 1.5.10.0.

In vivo confocal microscopy (IVCM) uses helium neon diode laser source with a wavelength of 670 nm. The two-dimensional images captured by the IVCM have a definition of 384 × 384 pixels over an area of 400 µm × 400 µm, with lateral spatial resolution of 0.5 µm and a depth resolution of 1–2 µm.

Data collection

Topical anaesthetic drops (Oxybuprocaine-Humacain 0.4%, Human Pharmaceuticals, Gödöllő, Hungary) were applied to the right eye and confocal cornea microscopy was carried out. Proper alignment and fixation of the eye was maintained with a target mobile red light for the contralateral eye. Sterile packaging disposable plastic cap (TomoCap®, Heidelberg, Germany) was used to keep the distance from the cornea to the microscope head stable. Carbomer gel (Vidisic; Dr Mann Pharma, Berlin, Germany) was used as coupling medium. Positioning of the objective lens was monitored with a digital camera tangential to the eye.

LCs were seen as hyper-reflective corpuscular particles with or without dendrite-like protrusions situated at the level of the basal epithelial cells and the sub-basal nerve plexus. We found LCs to have an average diameter of up to 15 µm in the corneal centre. LC densities were examined both at the centre of the cornea and its periphery at the 6 o’clock position at a depth of 40–60 µm from the corneal surface at the level of the basal epithelial cell layer and sub-basal nerve plexus. Forty images were taken and the five best-focused images were considered for the analysis in a masked fashion. After selection of the region of interest, cells could be marked and the system calculated cell density automatically (cell number/mm²). LC morphology (LCM) was evaluated on a 0–3 scale, where score 1 represented LCs without dendrites, score 2 was given to LCs with small processes and score 3 was given to LCs with long processes. Score 0 described the condition when the cornea was devoid of LCs. The average LCM was calculated in each of the figures selected and was used to describe the maturation of the LCs at both locations of the cornea (Figure 1).

Figure 1.

Confocal microscopic image of the corneal centre (A) and the periphery (C) in the control group. Note that central area is without obvious signs of the presence of Langerhans cells (LC) [LC morphology (LCM): score 0], while in the periphery some non-activated LCs (white arrow indicating a score 1 LC) can be seen accompanied by sub-basal nerves. (B) Corneal centre with gathering LCs with small processes (white arrowhead shows a score 2 LC). (D) Long and interdigitating LCs (empty arrow pointing at a score 3 LC) situated in a network-like fashion in the periphery indicating mature form of this cell type in the rheumatoid arthritis (RA) group.

Statistics

Data are expressed as mean ± SD. Comparisons between healthy individuals and RA patients, as well as between RA patient subgroups, were made with Cochran-Armitage trend tests in case of ordinal variables (LCM and LIPCOF). Continuous variables were compared using t-tests. Prior to analysis, the distribution of variables were checked graphically and, if necessary, variables were Box-Cox transformed prior to the analysis. We tested all possible two-way interactions (anti-TNF-α therapy*DAS28, DAS28*glucocorticosteroid, anti-TNF-α therapy *glucocorticosteroid) in the group of RA patients. None of these interactions were significant (details not shown). We used Spearman’s rank correlation test to investigate correlations within groups. P-values <0.05 were considered significant. Statistical analysis was performed using STATISTICA version 8.0 (StatSoft, Tulsa, OK, USA).

Results

The results of functional assays can be seen in Table 2. Of note, OSDI scores were higher and TBUT showed a trend to be lower than normal in RA (P = 0.057). Tear production showed a trend to be decreased only in RA patients on GCS therapy (P = 0.074).

Table 2.

Dry eye-related parameters in different subgroups of RA patients. Data are expressed as mean ± SD. Comparisons between healthy individuals and RA patients, as well as between RA patient subgroups, were made with Cochran-Armitage trend tests in the case of LIPCOF values. Continuous variables were compared using t-tests. Prior to analysis the distribution of variables was checked graphically and, if necessary, variables were Box-Cox transformed prior to the analysis.

Study group	OSDI	LIPCOF	Schirmer (mm/5 min)	TBUT [s]
Healthy individuals	11.71 ± 8.73	1.29 ± 0.55	11.96 ± 3.14	11.04 ± 3.32
All RA patients	24.46 ± 17.50^a	1.35 ± 0.68	9.74 ± 7.41	9.28 ± 3.86^c
RA patients according to DAS28 score
≤2.6 (53.8%)	25.83 ± 18.66	1.36 ± 0.68	10.23 ± 5.72	9.41 ± 3.50
>2.6 (46.2%)	22.87 ± 16.30	1.33 ± 0.70	9.17 ± 9.09	9.13 ± 4.32
RA patients according to anti-TNF-α therapy
Yes (44.2%)	28.28 ± 19.11	1.26 ± 0.62	9.63 ± 5.98	8.80 ± 3.54
No (55.8%)	21.44 ± 15.79	1.41 ± 0.73	9.83 ± 8.48	9.66 ± 4.12
RA patients according to glucocorticosteroid therapy
Yes (34.6%)	23.63 ± 15.83	1.39 ± 0.78	7.50 ± 5.50	8.83 ± 3.78
No (65.4%)	24.90 ± 18.54	1.32 ± 0.64	10.93 ± 8.06^b	9.52 ± 3.94

P < 0.05 versus healthy individuals.

P < 0.1 versus RA patients in the corresponding subgroup.

P < 0.1 versus healthy individuals.

Confocal microscopy data

The central and peripheral corneal LC prevalence values were higher in RA patients compared with healthy individuals (Table 3). The central LCM values were also higher than in controls. These data indicate that mature dendritic cells accumulate in the cornea of RA patients. The central LC density and the central LCM values were increased, even in RA patients in remission (<2.6 DAS28), as there was no difference between RA subgroups formed according to the clinical activity (DAS28).

Table 3.

Confocal microscopy results in different subgroups of RA patients. Data are expressed as mean ± SD. Comparisons between healthy individuals and RA patients, as well as between RA patient subgroups, were made with Cochran-Armitage trend tests in case of LCM values. Continuous variables were compared using t-tests. Prior to analysis the distribution of variables was checked graphically and, if necessary, variables were Box-Cox transformed prior to the analysis.

Study group	LC centre (cell/mm²)	LC periphery (cell/mm²)	LCM centre	LCM periphery
Healthy individuals	23.85 ± 33.81	69.29 ± 33.26	0.96 ± 0.75	2.42 ± 0.50
All RA patients	68.15 ± 71.27^a	126.8 ± 104.6^a	1.54 ± 0.78^a	2.60 ± 0.60
RA patients according to DAS28 score
≤2.6 (53.8%)	63.13 ± 66.20	134.3 ± 121.5	1.50 ± 0.75	2.68 ± 0.48
>2.6 (46.2%)	74.01 ± 77.80	117.9 ± 82.15	1.58 ± 0.83	2.50 ± 0.72
RA patients according to anti-TNF-α therapy
Yes (44.2%)	69.22 ± 69.61	124.8 ± 117.2	1.48 ± 0.67	2.65 ± 0.49
No (55.8%)	67.30 ± 73.78	128.3 ± 95.43	1.59 ± 0.87	2.55 ± 0.69
RA patients according to glucocorticosteroid therapy
Yes (34.6%)	37.37 ± 31.16	86.70 ± 47.16	1.50 ± 0.92	2.56 ± 0.78
No (65.4%)	84.45 ± 80.99^b	148.0 ± 120.0^c	1.56 ± 0.70	2.62 ± 0.49

P < 0.05 versus healthy individuals.

P < 0.1 versus RA patients in the corresponding subgroup.

P < 0.05 versus RA patients in the corresponding subgroup.

We also compared the LC density and morphology between RA subgroups formed according to therapy. LC density values were higher in RA patients without GCS therapy. In other words, GCS therapy restored the increased LC density observed in RA patients without GCS.

Discussion

To the best of our knowledge, this is the first study to investigate the characteristics of corneal LC density and morphology in RA. We have demonstrated increased density and activation of dendritic cells in the cornea of RA patients in the absence of clinically manifest ocular inflammation. This increased LC presence and activation did not appear to be associated with articular inflammatory disease activity, but correlated with the severity of hypolacrimation, and was abrogated by GCS therapy.

With the development of histochemistry and electron microscopy, a huge body of evidence was accumulated on corneal immunology, which required the revision of the tenet on the cornea as an immune privileged tissue.¹⁷ Various immune cells were demonstrated to reside in the cornea, including LCs.⁷ In healthy conditions, LCs are scarce in the centre of the cornea. Upon different triggers, however, LCs migrate to the centre of the cornea and transform into an active participant of the corneal immune response by the formation of dendrite-like processes and expression of co-stimulatory molecules, including CD80 and CD86.¹⁸ LCs are found in a greater number in several inflammation-related conditions, including contact lens wearers³ and Thygeson’s superficial punctate keratitis,^8,9 and also in experimental conditions.^19,20 The elevation of LC and leukocyte density both in the centre and the periphery of the cornea has already been described in patients with Sjögren’s syndrome.²¹ In this study we have used confocal microscopy, a recently developed device that is non-invasive and capable of visualizing the ultrastructure of the ocular surface, including the meibomian glands at a cell level.²² Reliability and specificity of the device have been acknowledged in a study by Imre et al.;²³ however, there are some limitations when it is used on corneas with decreased transparency. We aimed to investigate the density and morphology of corneal LCs for their presumed role in ocular surface diseases and their properties to indicate the corneal homeostasis. LCs reside almost exclusively in the superficial cornea and can be distinguished from leukocytes through their appearance. They have an extraordinary capacity to stimulate naïve T cells and are recognized as essential regulators of both the innate and acquired arms of the immune system.^7,21 We have observed that, in contrast with healthy subjects, LC density was elevated markedly and found to reside in the corneal centre of RA patients, even without overlapping Sjögren’s syndrome or in the absence of overt eye symptoms. Additionally, more than half of these LCs showed an activated phenotype with small or long projections.

It has been shown that the recruitment and maturation of LCs can be induced by several pro-inflammatory cytokines, including IL-1α, TNF-α, IL-6, IL-8 and IL-12.^10,23 Both IL-1 inhibitors, anti-TNF-α therapy and GCS suppressed the LC migration in vitro effectively.^24,25 Our clinical results also suggest this possible inhibitory effect of GCS therapy on the activation of LCs in RA.

Corneal immune status may be strongly interrelated with dysfunctional tear production, but the causative relationship has still not been established. It has long been known that dry eye is more common among patients with autoimmune diseases,¹ but the precise pathophysiologic mechanism is still unclear. Hyposecretory conditions, such as Sjögren’s syndrome, through the reduced moisturization of the ocular surface, may initiate or contribute to the development of dry eye. Corneal morphological changes like thinning of the cornea, lower density of superficial epithelial cells, fewer sub-basal nerves and greater nerve tortuosity have been described in association with dry eye²⁶ and in RA subjects.²⁷ Inadequate moisturization leads to increased apoptosis and further induction of pro-inflammatory cytokines, including IL-1, 6, 8 and TNF-α, which have been found to be overexpressed and to accumulate in the ocular surface. In turn, these cytokines are thought to have the capacity to decrease tear production via neuronal and hormonal effects.^28,29 Indeed, we found decreased tear production in RA patients who had at least moderate RA activity. Theoretically, higher clinical activity in RA results in higher systemic inflammation, which may also increase the secretion of pro-inflammatory cytokines in tears. The possible higher amount of these cytokines in the tears of RA patients with higher disease activity might impair tear production and it might partly explain the dry eye mechanism without the presence of true overlapping Sjögren’s syndrome. It is of importance to emphasize that none of the RA patients had overlapping Sjögren’s syndrome. Our results are in accordance with the results of Villani et al.,²⁷ which is of particular interest because some reports suggest that there are profound aetiologic and pathogenic differences between keratoconjunctivitis sicca in patients with RA with secondary Sjögren’s syndrome, and patients with RA without secondary Sjögren’s, though they lack manifest differences in the clinical indicators.³⁰ Rather, our data, along with that of Villani et al.,²⁷ suggest that these alterations of the cornea are associated with the systemic inflammatory effect of the disease than a specific pathogenic difference in KCS in patients with or without Sjögren’s syndrome. Also, our data, together with that of Villani et al., ²⁷ may lend itself to the identification of some indices of disease activity on the ocular surface that could be compared with the indices of activity of the systemic disease. Our results are also in agreement with previous results, which showed that ocular surface LCs are essential for T cell-mediated dry eye.³¹ Our results also support the systemic multi-organ-related feature of RA affecting the eye. Recent data showed an increased accumulation of dendritic cells (DCs) in the synovial fluid of patients with active RA and the decrease in DCs in the peripheral blood. Because DCs migrate to sites of inflammation, lack of them in the peripheral blood of patients with active RA may be owing to the recruitment of DCs at the synovium. According to our results a similar process might act also in the cornea of patients with mild or moderate active RA.³² We have also demonstrated that low-dose, continuously-used oral GCS therapy can significantly reduce the density of LCs, both in the central and peripheral parts of the cornea. Low-dose, continuously-used oral GCS therapy also inhibits the dendrite-forming ability of central LCs. These results also suggest that the immunosuppressive effects of GCS also affect the corneal immune mechanisms in RA.

Footnotes

Funding

Attila Balog and Gergely Toldi were supported by the Magyary Zoltán Hungarian Scientific Scholarship (Grant no. TÁMOP-4.2.4. A/2-11-1-2012-001).

References

Lemp

. Dry eye (keratoconjunctivitis sicca), rheumatoid arthritis, and Sjögren’s syndrome. Am J Ophthalmol 2005; 140: 898–899.

Resch

Imre

Tapasztó

Németh

. Confocal microscopic evidence of increased Langerhans cell activity after corneal metal foreign body removal. Eur J Ophthalmol 2008; 18: 703–707.

Zhivov

Stave

Vollmar

Guthoff

. In vivo confocal microscopic evaluation of Langerhans cell density and distribution in the corneal epithelium of healthy volunteers and contact lens wearers. Cornea 2007; 26: 47–54.

Hamrah

Liu

Zhang

Dana

. Alterations in corneal stromal dendritic cell phenotype and distribution in inflammation. Arch Ophthalmol 2003; 121: 1132–1140.

Seto

Gillette

Chandler

. HLA-DR+/T6- Langerhans cells of the human cornea. Invest Ophthalmol Vis Sci 1987; 28: 1719–1722.

Zhivov

Stave

Vollmar

Guthoff

. In vivo confocal microscopic evaluation of Langerhans cells density and distribution in the normal corneal epithelium. Graefe’s Arch Clin Exp Ophthalmol 2005; 243: 1056–1061.

Hamrah

Dana

. Corneal antigen-presenting cells. Chem Immunol Allergy 2007; 92: 58–70.

Kawamoto

Chikama

Takahashi

Nishida

. In vivo observation of Langerhans cells by laser confocal microscopy in Thygeson's superficial punctate keratitis. Mol Vis 2009; 29: 1456–1462.

Chen

Han

Chen

. Dendritiform cells found in central cornea by in-vivo confocal microscopy in a patient with mixed bacterial keratitis. Ocul Immunol Inflamm 2006; 14: 241–244.

10.

Dekaris

Zhu

Dana

. TNF-alpha regulates corneal Langerhans cell migration. J Immunol 1999; 162: 4235–4239.

11.

Niederkorn

Peeler

Mellon

. Phagocytosis of particulate antigens by corneal epithelial cells stimulate interleukin-1 secretion and migration of Langerhans cells into the central cornea. Reg Immunol 1989; 2: 83–90.

12.

Minsky

. Memoir on inventing the confocal scanning microscope. Scanning 1988; 10: 128–138.

13.

Aletaha

Neogi

Silman

. Rheumatoid arthritis classification criteria: an American College of Rheumatology/European League Against Rheumatism collaborative initiative. Arthritis Rheum 2010; 62: 2569–2581.

14.

Vitali

Bombardieri

Jonsson

. European Study Group on Classification Criteria for Sjögren's Syndrome. Classification criteria for Sjögren's syndrome: a revised version of the European criteria proposed by the American–European Consensus Group. Ann Rheum Dis 2002; 61: 554–558.

15.

Schiffman

Christianson

Jacobsen

. Reliability and validity of the Ocular Surface Disease Index. Arch Ophthalmol 2000; 118: 615–621.

16.

Pult

Purslow

Murphy

. The relationship between clinical signs and dry eye symptoms. Eye 2011; 25: 502–510.

17.

Gillette

Chandler

Greiner

. Langerhans cells of the ocular surface. Ophthalmology 1982; 89: 700–711.

18.

Hamrah

Huq

Liu

. Corneal immunity is mediated by heterogenous population of antigen-presenting cells. J Leukoc Biol 2003; 73: 172–178.

19.

Zhivov

Kraak

Bergter

. Influence of benzalkonium chloride on Langerhans cells in corneal epithelium and development of dry eye in healthy volunteers. Curr Eye Res 2010; 35: 762–769.

20.

Chen

Lin

Dong

. Cauterization of central cornea induces recruitment of major histocompatibility complex class II + Langerhans cells from limbal basal epithelium. Cornea 2010; 29: 73–79.

21.

Lin

Dong

. Changes in corneal epithelial layer inflammatory cells in aqueous tear-deficient dry eye. Invest Ohpthalmol Vis Sci 2010; 51: 122–128.

22.

Villani

Beretta

De Capitani

. In vivo confocal microscopy of meibomian glands in Sjögren's syndrome. Invest Ophthalmol Vis Sci 2011; 52: 933–939.

23.

Imre

Nagymihály

. Reliability and reproducibility of corneal endothelial image analysis by in vivo confocal microscopy. Graefes Arch Clin Exp Ophtalmol 2001; 239: 356–360.

24.

Dana

Dai

. Wayne. Interleukin-1 receptor antagonist suppresses Langerhans cell activity and promotes ocular immune privilege. Invest Ohpthalmol Vis Sci 1998; 39: 70–77.

25.

Dana

. Comparison of topical interleukin-1 vs tumor necrosis factor-alpha blockade with corticosteroid therapy on murine corneal inflammation, neovascularization, and transplant survival (an American Ophthalmological Society thesis). Trans Am Ophthalmol Soc 2007; 105: 330–343.

26.

Erdélyi

Kraak

Zhivov

. In vivo confocal laser scanning microscopy of the cornea in dry eye. Graefes Arch Clin Exp Ophthalmol 2007; 245: 39–44.

27.

Villani

Galimberti

Viola

. Corneal involvement in rheumatoid artritis: an in vivo confocal study. Invest Ohpthalmol Vis Sci 2008; 49: 560–564.

28.

Pitcher

JD 3rd

De Paiva

Pelegrino

. Pharmacological cholinergic blockade stimulates inflammatory cytokine production and lymphocytic infiltration in the mouse lacrimal gland. Invest Ophthalmol Vis Sci 2011; 52: 3221–3227.

29.

Massingale

Vallabhajosyula

. Analysis of inflammatory cytokines in the tears of dry eye patients. Cornea 2009; 28: 1023–1027.

30.

Fujita

Igarashi

Kurai

. Correlation between dry eye and rheumatoid arthritis activity. Am J Ophthalmol 2005; 140: 808–813.

31.

Stern

Wheeler

Niederkorn

. Ocular surface APCs are necessary for autoreactive T cell-mediated experimental autoimmune lacrimal keratoconjunctivitis. J Immunol 2011; 187: 3653–3662.

32.

Kavousanaki

Makrigiannakis

Boumpas

Verginis

. Novel role of plasmocytoid dendritic cells in human induction of interleukin-10 producing Treg cells by plasmocytoid dendritic cells in patients with rheumatoid arthritis responding to therapy. Arthritis Rheum 2010; 62: 53–63.

In vivo confocal microscopic evaluation of corneal Langerhans cell density,and distribution and evaluation of dry eye in rheumatoid arthritis

Abstract

Keywords

Introduction

Materials and methods

Patients

Eye examinations

Dry eye examinations

In vivo confocal microscopy investigations

Data collection

Statistics

Results

Confocal microscopy data

Discussion

Footnotes

Funding

References