CD4 + Count: a Variable to Be Considered to Prioritize COVID-19 Vaccination in PLHIV.

Q1 Biochemistry, Genetics and Molecular Biology Current Pharmacology Reports Pub Date : 2023-01-01 DOI:10.1007/s40495-023-00312-4
Vakada Lakshmi Mounika, V Udaya Kumar, Sameer Dhingra, V Ravichandiran, Krishna Pandey, Vipan Kumar Parihar, Krishna Murti
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Abstract

The outbreak of the COVID-19 propagates, pressurizing the healthcare system by emphasizing and worsening the inequities. While many vaccines have shown excellent efficacy in protecting the general public from the COVID-19 infection, the efficacy of these vaccines for people living with HIV (PLHIV), especially those having a different range of CD4 + T-cell, has yet to be thoroughly investigated. Few studies have uncovered the escalated infection and death rates due to the COVID-19 infection in individuals with low CD4 + T-cells. Additionally, PLHIV has a low CD4 + count; furthermore, specific CD4 + T cells for coronavirus have a vigorous Th1 role and are related to the protective antibody responses. Follicular helper T cells (TFH) are vulnerable to HIV and virus-specific CD4 & CD8 T-cells which are essential for viral infection clearance and defective immune responses which further contributes to the development of illness. The specific CD8 & CD4 + T-cell reaction to severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) was identified in almost all COVID-19 recovered individuals, which is related to the size of antibodies of immunoglobulin G. It has previously been demonstrated that PLHIV has decreased responses to certain vaccines and that these responses are reliant on CD4 + T-cell levels. COVID-19 vaccines will likely have a lower response or limited effect, in PLHIV having low CD4 + T-cells.

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CD4 +计数:在PLHIV中优先考虑COVID-19疫苗接种的一个变量
新型冠状病毒感染症(COVID-19)的扩散加剧了不公平现象,给医疗保健系统带来了压力。虽然许多疫苗在保护公众免受COVID-19感染方面显示出极好的功效,但这些疫苗对艾滋病毒感染者(PLHIV)的功效,特别是对那些CD4 + t细胞范围不同的人的功效,尚未得到彻底调查。很少有研究发现CD4 + t细胞水平低的个体感染COVID-19导致的感染率和死亡率上升。此外,PLHIV具有较低的CD4 +计数;此外,针对冠状病毒的特异性CD4 + T细胞具有强烈的Th1作用,并与保护性抗体反应有关。滤泡辅助性T细胞(TFH)容易受到HIV和病毒特异性CD4和CD8 T细胞的攻击,这对于病毒感染清除和缺陷免疫反应至关重要,从而进一步促进疾病的发展。在几乎所有COVID-19康复个体中都发现了对严重急性呼吸综合征-冠状病毒2 (SARS-CoV-2)的特异性CD8和CD4 + t细胞反应,这与免疫球蛋白g抗体的大小有关。先前已经证明,PLHIV降低了对某些疫苗的反应,并且这些反应依赖于CD4 + t细胞水平。对于CD4 + t细胞较低的PLHIV病毒,COVID-19疫苗的反应可能较低或效果有限。
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来源期刊
Current Pharmacology Reports
Current Pharmacology Reports Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
9.30
自引率
0.00%
发文量
35
期刊介绍: Current Pharmacology Reports will: publish cutting-edge reviews on subjects pertinent to all aspects of pharmacology, including drug discovery and development.provide incisive, insightful, and balanced contributions from international leading experts.interest a wide readership of basic scientists and translational investigators in academia and in industry. The Current Pharmacology Reports journal accomplishes its goal by appointing international authorities to serve as Section Editors in key subject areas, such as: epigenetics and epigenomics, chemoinformatics and rational drug design and target discovery, drug delivery and biomaterial, pharmacogenomics and molecular targets and biomarkers, chemical/drug/molecular toxicology, absorption, distribution, metabolism and elimination (ADME), pharmacokinetics (PK) and pharmacodynamics (PD), Modeling & Simulation (M&S) and pharmacometrics, and other related topics in pharmacology including neurology/central nervous system (CNS), cardiovascular, metabolic diseases, cancer, among others. Section Editors for Current Pharmacology Reports select topics for which leading experts contribute comprehensive review articles that emphasize new developments and recently published papers of major importance, highlighted by annotated reference lists. An Editorial Board of internationally diverse members suggests topics of special interest to their country/region and ensures that topics are current and include emerging research. Commentaries from well-known figures in the field are also provided. This journal publishes on a bi-monthly schedule.Please submit here: https://www.editorialmanager.com/phar/default.aspx
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