Epling Brian P, Lisco Andrea, Manion Maura, Laidlaw Elizabeth, Galindo Frances, Anderson Megan, Roby Gregg, Sheikh Virginia, Migueles Stephen A, Poole April, Perez-Diez Ainhoa, Liu Xiangdong, Rao V Koneti, Burbelo Peter D, Sereti Irini
Laboratory of Immunoregulation.
Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases.
Clin Infect Dis. 2025 Jul 18;80(6):1340-1348. doi: 10.1093/cid/ciae562.
Despite suppressive antiretroviral therapy (ART), 15%-30% of people with human immunodeficiency virus (HIV) experience a limited recovery of CD4 T cells. Although autoantibodies against the CD4 receptor have previously been identified in people with HIV (PWH), little is known about their longitudinal impact on CD4 T-cell reconstitution.
Anti-CD4 autoantibodies were evaluated by the fluid-phase luciferase immunoprecipitation systems immunoassay in ART-naive people with advanced HIV (CD4 count ≤100 cells/µL), PWH with CD4 count >200 cells/µL, long-term nonprogressors, people with idiopathic CD4 lymphopenia, people with autoimmune lymphoproliferative syndrome, and healthy volunteers without HIV. In the participants with advanced HIV, we assessed the association of anti-CD4 autoantibodies at ART initiation with CD4 recovery over a median follow-up of 192 weeks.
Anti-CD4 autoantibodies were identified in 29% (61/210) of ART-naive participants with advanced HIV but were absent in people without HIV. Female PWH showed a 4-fold higher prevalence (P < .001) of anti-CD4 autoantibodies compared to males. After ART initiation, people with advanced HIV with anti-CD4 autoantibodies exhibited an overall slower rate of CD4 reconstitution (5.8 vs 6.6 cells/µL/month, P = .007) and lower week 192 CD4 count (268 vs 355 cells/µL, P = .037). Incidental, clinically indicated immunosuppressive therapy in these participants was associated with an improved rate of CD4 reconstitution (P = .0019) and higher week 192 CD4 count (551 vs 268 cells/µL, P = .019).
People with advanced HIV harboring anti-CD4 autoantibodies at ART initiation demonstrated a slower rate and extent of CD4 reconstitution after 4 years. Incidental immunosuppressive therapy was associated with increased CD4 counts in these participants.
尽管接受了抗逆转录病毒抑制疗法(ART),但仍有15%-30%的人类免疫缺陷病毒(HIV)感染者的CD4 T细胞恢复有限。虽然先前已在HIV感染者(PWH)中鉴定出针对CD4受体的自身抗体,但对其对CD4 T细胞重建的纵向影响知之甚少。
通过液相荧光素酶免疫沉淀系统免疫测定法,对未接受过ART治疗的晚期HIV感染者(CD4细胞计数≤100个/µL)、CD4细胞计数>200个/µL的PWH、长期不进展者、特发性CD4淋巴细胞减少症患者、自身免疫性淋巴增生综合征患者以及无HIV的健康志愿者进行抗CD4自身抗体评估。在晚期HIV感染者中,我们评估了ART开始时抗CD4自身抗体与192周中位随访期内CD4恢复情况之间的关联。
在未接受过ART治疗的晚期HIV感染者中,29%(61/210)检测出抗CD4自身抗体,而无HIV者未检测到。女性PWH抗CD4自身抗体的患病率比男性高4倍(P<.001)。开始ART治疗后,有抗CD4自身抗体的晚期HIV感染者的CD4重建总体速度较慢(5.8 vs 6.6个/µL/月,P=.007),且第192周时的CD4细胞计数较低(268 vs 355个/µL,P=.037)。这些参与者偶然接受的临床指示性免疫抑制治疗与CD4重建速度加快(P=.0019)和第192周时更高CD4细胞计数(551 vs 268个/µL,P=.019)相关。
开始ART治疗时携带抗CD4自身抗体的晚期HIV感染者在4年后的CD4重建速度和程度较慢。偶然的免疫抑制治疗与这些参与者CD4细胞计数增加相关。