1Division of Comparative Pathology, Covington, Louisiana.
2Division of Microbiology, Tulane National Primate Research Center, Covington, Louisiana, USA.
J Gen Virol. 2019 Jan;100(1):26-34. doi: 10.1099/jgv.0.001181. Epub 2018 Nov 29.
For an effective T-cell activation and response, co-stimulation is required in addition to the antigen-specific signal from their antigen receptors. The CD2/CD58 interaction is considered as one of the most important T-cell co-stimulatory pathways for T-cell activation and proliferation, and its role in regulating intestinal T-cell function in acute and chronic SIV -infected macaques is poorly documented. Here, we demonstrated a significant reduction of CD58 expression in both T- and B-cell populations during acute SIV infection along with high plasma viral load and a loss of intestinal CD4 T cells compared to SIV-uninfected control macaques. The reduction of CD58 expression in T cells was correlated with the reduced expression of T-cell-mediated IL-2 and TNFα production. Together, these results indicate that reduction in the CD2/CD58 interaction pathway in mucosal lymphocytes might play a crucial role in mucosal T-cell dysfunction during acute SIV/HIV infection.
为了实现有效的 T 细胞激活和应答,除了抗原受体的抗原特异性信号外,还需要共刺激。CD2/CD58 相互作用被认为是 T 细胞激活和增殖的最重要的共刺激途径之一,但其在调节急性和慢性 SIV 感染猕猴肠道 T 细胞功能中的作用尚未得到充分记录。在这里,我们发现在急性 SIV 感染期间,T 细胞和 B 细胞群体中的 CD58 表达显著降低,与 SIV 未感染对照猕猴相比,血浆病毒载量高,并且肠道 CD4 T 细胞丢失。T 细胞中 CD58 表达的减少与 T 细胞介导的 IL-2 和 TNFα 产生的表达减少相关。总之,这些结果表明,粘膜淋巴细胞中 CD2/CD58 相互作用途径的减少可能在急性 SIV/HIV 感染期间粘膜 T 细胞功能障碍中起关键作用。