Nebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, NE 68583; and School of Biological Sciences, University of Nebraska-Lincoln, Lincoln, NE 68583.
Nebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, NE 68583; and School of Biological Sciences, University of Nebraska-Lincoln, Lincoln, NE 68583
J Immunol. 2018 May 1;200(9):3180-3187. doi: 10.4049/jimmunol.1701288. Epub 2018 Apr 2.
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) cells, and T follicular regulatory (T) 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/T 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 cells, T 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/T cells in SIV infection correlated with anti-dsDNA and anti-phospholipid autoreactive Ab levels, whereas the frequency of T cells alone did not correlate with the levels of autoreactive Abs. Our results provide direct evidence that the ratio of T/T cells in LTs is critical for regulating autoreactive Ab production in chronic SIV infection and possibly, by extension, in chronic HIV-1 infection.
慢性 HIV-1 感染个体的自身反应性 Abs 发生率增加。从这些个体中分离出的许多 HIV 广谱中和 Abs 也是自身反应性的。然而,产生这些自身反应性广谱中和 Abs 的潜在机制仍很大程度上未知。外周淋巴组织(LTs)生发中心(GCs)中 B 细胞、滤泡辅助 T(Tfh)细胞和滤泡调节 T(Tfr)细胞之间高度调节的协调对于防御病原体至关重要,同时也限制了自身反应性应答。我们假设 GC 中 T/T 细胞的比例改变导致慢性 HIV 感染中自身反应性 Abs 的发生率增加。我们使用恒河猴(RM)SIV 模型来检验这一假设。我们测量了 LTs 中 T 细胞、Tfh 细胞和 GC B 细胞的频率以及来自感染和未感染 SIV 的印度 RM 的抗 dsDNA 和抗磷脂 Abs。我们发现慢性感染的 RM(83.3%[5/6]和 66.7%[4/6])中抗 dsDNA 和抗磷脂 Abs 的频率明显高于急性感染的 RM(33.3%[2/6]和 18.6%[1/6])和未感染的 RM(0%[0/6]和 18.6%[1/6])。SIV 感染中 T/T 细胞比例的增加与抗 dsDNA 和抗磷脂自身反应性 Ab 水平相关,而 T 细胞的频率与自身反应性 Abs 水平无关。我们的结果提供了直接证据,表明 LTs 中 T/T 细胞的比例对于调节慢性 SIV 感染中的自身反应性 Ab 产生至关重要,并且可能在慢性 HIV-1 感染中也是如此。