Abstract
Objectives
Lymphocytes are key players in the adaptive immune system, playing an important role in the anti-inflammatory balance in the post-myocardial infarction (MI) period and being involved in healing process. We aimed to investigate temporal changes in lymphocyte subunits in maladaptive remodeling following acute myocardial infarction.
Design and setting
A total of 84 patients with anterior ST-segment elevation MI (STEMI) were enrolled. Lymphocyte subunits were measured 1 day, 2 and 6 weeks after MI. Maladaptive cardiac remodeling was defined as an increase in left ventricular end-diastolic volume by ≥12% in cardiac magnetic resonance imaging at the 6-months follow-up.
Participants
A total of 84 patients with anterior STEMI were enrolled.
Measurements and results
On the first day post-MI, the median number of total lymphocytes, T cells, and B cells were higher in the maladaptive remodeling group than in the without maladaptive remodeling group. Two weeks post-MI, the median number of B cells was higher in the maladaptive remodeling group, but similar at 6 weeks post-MI. Regression analysis revealed that a high number of B cells on the first day post-MI was related to maladaptive remodeling.
Conclusions
In the maladaptive remodeling group, both inflammation markers, T and B lymphocyte levels were higher in the initial phase of MI, while B cells were approximately two-fold higher and an independent predictor of maladaptive remodeling. This study strongly supports the idea of developing immunotherapies or treatments that target B cells in cardiac remodeling.
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