Hokello Joseph, Tyagi Kratika, Owor Richard Oriko, Sharma Adhikarimayum Lakhikumar, Bhushan Alok, Daniel Rene, Tyagi Mudit
Department of Biology, Faculty of Science and Education, Busitema University, Tororo P.O. Box 236, Uganda.
Department of Biotechnology, Banasthali Vidyapith, Jaipur 304022, India.
Life (Basel). 2024 Jan 9;14(1):104. doi: 10.3390/life14010104.
The theory of immune regulation involves a homeostatic balance between T-helper 1 (Th1) and T-helper 2 (Th2) responses. The Th1 and Th2 theories were introduced in 1986 as a result of studies in mice, whereby T-helper cell subsets were found to direct different immune response pathways. Subsequently, this hypothesis was extended to human immunity, with Th1 cells mediating cellular immunity to fight intracellular pathogens, while Th2 cells mediated humoral immunity to fight extracellular pathogens. Several disease conditions were later found to tilt the balance between Th1 and Th2 immune response pathways, including HIV infection, but the exact mechanism for the shift from Th1 to Th2 cells was poorly understood. This review provides new insights into the molecular biology of HIV, wherein the HIV life cycle is discussed in detail. Insights into the possible mechanism for the Th1 to Th2 shift during HIV infection and the preferential infection of Th2 cells during the late symptomatic stage of HIV disease are also discussed.
免疫调节理论涉及辅助性T细胞1(Th1)和辅助性T细胞2(Th2)反应之间的稳态平衡。Th1和Th2理论于1986年在对小鼠的研究中提出,当时发现辅助性T细胞亚群可引导不同的免疫反应途径。随后,这一假说扩展到人类免疫,Th1细胞介导细胞免疫以对抗细胞内病原体,而Th2细胞介导体液免疫以对抗细胞外病原体。后来发现几种疾病状态会使Th1和Th2免疫反应途径之间的平衡发生倾斜,包括HIV感染,但从Th1细胞向Th2细胞转变的确切机制尚不清楚。本综述为HIV的分子生物学提供了新见解,其中详细讨论了HIV的生命周期。还讨论了对HIV感染期间Th1向Th2转变的可能机制以及HIV疾病晚期症状阶段Th2细胞优先感染的见解。