TY - JOUR
T1 - Altered ratio of t follicular helper cells to t follicular regulatory cells correlates with autoreactive antibody response in simian immunodeficiency virus–Infected rhesus macaques
AU - Fan, Wenjin
AU - Demers, Andrew James
AU - Wan, Yanmin
AU - Li, Qingsheng
N1 - Funding Information:
This work was supported by National Institutes of Health Grant R01 DK087625-01 (to Q.L.), National Center for Research Resources Grant 5P30RR031151-03, and National Institute of General Medical Sciences Grant 8 P30 GM103509-03.
Publisher Copyright:
Copyright © 2018 by The American Association of Immunologists, Inc.
PY - 2018/5/1
Y1 - 2018/5/1
N2 - Individuals with chronic HIV-1 infection have an increased prevalence of autoreactive Abs. Many of the isolated HIV broadly neutralizing Abs from these individuals are also autoreactive. However, the underlying mechanism(s) that produce these autoreactive broadly neutralizing Abs remains largely unknown. The highly regulated coordination among B cells, T follicular helper (T FH ) cells, and T follicular regulatory (T FR ) cells in germinal centers (GCs) of peripheral lymphatic tissues (LTs) is essential for defense against pathogens while also restricting autoreactive responses. We hypothesized that an altered ratio of T FH /T FR cells in the GC contributes to the increased prevalence of autoreactive Abs in chronic HIV infection. We tested this hypothesis using a rhesus macaque (RM) SIV model. We measured the frequency of T FH cells, T FR cells, and GC B cells in LTs and anti-dsDNA and anti-phospholipid Abs from Indian RMs, with and without SIV infection. We found that the frequency of anti-dsDNA and anti-phospholipid Abs was much higher in chronically infected RMs (83.3% [5/6] and 66.7% [4/6]) than in acutely infected RMs (33.3% [2/6] and 18.6% [1/6]) and uninfected RMs (0% [0/6] and 18.6% [1/6]). The increased ratio of T FH /T FR cells in SIV infection correlated with anti-dsDNA and anti-phospholipid autoreactive Ab levels, whereas the frequency of T FR cells alone did not correlate with the levels of autoreactive Abs. Our results provide direct evidence that the ratio of T FH /T FR cells in LTs is critical for regulating autoreactive Ab production in chronic SIV infection and possibly, by extension, in chronic HIV-1 infection. The Journal of Immunology, 2018, 200: 3180–3187.
AB - Individuals with chronic HIV-1 infection have an increased prevalence of autoreactive Abs. Many of the isolated HIV broadly neutralizing Abs from these individuals are also autoreactive. However, the underlying mechanism(s) that produce these autoreactive broadly neutralizing Abs remains largely unknown. The highly regulated coordination among B cells, T follicular helper (T FH ) cells, and T follicular regulatory (T FR ) cells in germinal centers (GCs) of peripheral lymphatic tissues (LTs) is essential for defense against pathogens while also restricting autoreactive responses. We hypothesized that an altered ratio of T FH /T FR cells in the GC contributes to the increased prevalence of autoreactive Abs in chronic HIV infection. We tested this hypothesis using a rhesus macaque (RM) SIV model. We measured the frequency of T FH cells, T FR cells, and GC B cells in LTs and anti-dsDNA and anti-phospholipid Abs from Indian RMs, with and without SIV infection. We found that the frequency of anti-dsDNA and anti-phospholipid Abs was much higher in chronically infected RMs (83.3% [5/6] and 66.7% [4/6]) than in acutely infected RMs (33.3% [2/6] and 18.6% [1/6]) and uninfected RMs (0% [0/6] and 18.6% [1/6]). The increased ratio of T FH /T FR cells in SIV infection correlated with anti-dsDNA and anti-phospholipid autoreactive Ab levels, whereas the frequency of T FR cells alone did not correlate with the levels of autoreactive Abs. Our results provide direct evidence that the ratio of T FH /T FR cells in LTs is critical for regulating autoreactive Ab production in chronic SIV infection and possibly, by extension, in chronic HIV-1 infection. The Journal of Immunology, 2018, 200: 3180–3187.
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U2 - 10.4049/jimmunol.1701288
DO - 10.4049/jimmunol.1701288
M3 - Article
C2 - 29610141
AN - SCOPUS:85046284507
SN - 0022-1767
VL - 200
SP - 3180
EP - 3187
JO - Journal of Immunology
JF - Journal of Immunology
IS - 9
ER -