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Common Variable Immunodeficiency and Circulating TFH
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DOI：10.1155/2016/4951587.png)
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Abstract
En 中文
CD4+ T follicular helper cells (T-FH) were assessed in adult patients with common variable immune deficiency (CVID) classified according to the presence of granulomatous disease (GD), autoimmunity (AI), or both GD and AI (Group I) or the absence of AI and GD (Group II). T-FH lymphocytes were characterized by expression of CXCR5 and PD-1. T-FH were higher (in both absolute number and percentage) in Group I than in Group II CVID patients and normal controls (N). Within CXCR5+CD4+ T cells, the percentage of PD-1 (+) was higher and that of CCR7 (+) was lower in Group I than in Group II and N. The percentages of Treg and T-FH reg were similar in both CVID groups and in N. T-FH responded to stimulation increasing the expression of the costimulatory molecules CD40L and ICOS as did N. After submitogenic PHA+IL-2 stimulation, intracellular expression of T-FH cytokines (IL-10, IL-21) was higher than N in Group I, and IL-4 was higher than N in Group II. These results suggest that T-FH are functional in CVID and highlight the association of increased circulating T-FH with AI and GD manifestations.
Keywords:
ANTIBODY-DEFICIENCY SYNDROME
CHRONIC VIRAL-INFECTION
B-CELLS
SYSTEMIC AUTOIMMUNITY
IGA DEFICIENCY
MUTATIONS
TACI
PD-1
LYMPHOCYTES
GENERATION
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