Cellular Immune Response to High-Risk Human Papillomavirus Infection: A Systematic Review.

IF 0.8 4区 医学 Q4 IMMUNOLOGY
Danielle Oliveira da Fonseca, Marco Antonio Moreira Puga, Vanessa T Gubert, Erica Freire de Vasconcelos Pereira, Vanessa Marcon de Oliveira, Maxlainy Tosta, Mariana Vidotti de Jesus, Inês Aparecida Tozetti
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引用次数: 0

Abstract

The relationship between human papillomavirus (HPV) and immune cells is vital for understanding the pathophysiology of infection and its role in neoplastic progression. High-risk human papillomavirus (HR-HPV) is the main cause of cervical cancer (CC). Thus, the association between immune response cells, the virus, and its behavior according to cervical disease development could provide new ways for understanding the entire process. Since the role and the presence of the immune response cells in the uterus cervix considering HPV infection has not been elucidated so far, this study aimed to identify the immune cells involved in high-grade intraepithelial lesions (HSIL) and CC development related to uterine cervical infection caused by HR-HPV. The study population included women who had positive molecular tests for HPV. Through the databases MEDLINE, EMBASE, LILACS, Cochrane, Scopus, Web of Science, CINAHL, Science Direct, and Google Scholar we identified 6,698 studies at the beginning. After the systematic review steps, the final number of included studies was 22. Cervical lesions were distributed according to the severity of lesions in HSIL, low-grade squamous intraepithelial lesions (LSIL), and negative for intraepithelial lesions or malignancy (NILM). The cellular phenotypes presented in these publications were T lymphocytes (LT), regulatory T lymphocytes (Tregs), macrophages (MØ), natural killer cells (NK), natural killer T cells (NKT), Langerhans cells (LC), and dendritic cells (DC). Among the observed associations with cervical lesions and HR-HPV, we highlight the DC/LC and MØ being 36.4% of the cell types, followed by Tregs (31.8%) and LT CD4 / CD8 with 27.3%. The increased findings in innate and adaptive immunological response may imply both are acting together, with the innate response cells and Tregs being the most prominent. Since these cells have great importance in the maintenance and balance of the immunological system, the present study highlights the essential role of MØ and Treg cells in the process of cervical lesion severity associated with HPV, suggesting that they may be focused as prognostic markers and immunotherapeutic targets.

高危人乳头瘤病毒感染的细胞免疫反应:系统综述。
人乳头瘤病毒(HPV)和免疫细胞之间的关系对于理解感染的病理生理及其在肿瘤进展中的作用至关重要。高危人乳头瘤病毒(HR-HPV)是宫颈癌(CC)的主要病因。因此,根据宫颈疾病的发展,免疫反应细胞、病毒及其行为之间的联系可以为理解整个过程提供新的途径。由于考虑HPV感染的宫颈免疫应答细胞的作用和存在至今尚未阐明,本研究旨在鉴定与HR-HPV引起的宫颈感染相关的高级别上皮内病变(HSIL)和CC发展相关的免疫细胞。研究人群包括HPV分子检测呈阳性的妇女。通过MEDLINE、EMBASE、LILACS、Cochrane、Scopus、Web of Science、CINAHL、Science Direct和b谷歌Scholar等数据库,我们一开始确定了6698项研究。经过系统评价步骤,最终纳入的研究数量为22项。宫颈病变按病变严重程度分为HSIL、低级别鳞状上皮内病变(LSIL)、上皮内病变阴性或恶性病变(NILM)。这些出版物中出现的细胞表型包括T淋巴细胞(LT)、调节性T淋巴细胞(Tregs)、巨噬细胞(MØ)、自然杀伤细胞(NK)、自然杀伤T细胞(NKT)、朗格汉斯细胞(LC)和树突状细胞(DC)。在观察到的与宫颈病变和HR-HPV相关的细胞类型中,我们强调DC/LC和MØ占36.4%,其次是Tregs(31.8%)和LT CD4 / CD8(27.3%)。先天免疫反应和适应性免疫反应的增加可能意味着两者共同作用,先天反应细胞和Tregs是最突出的。由于这些细胞在免疫系统的维持和平衡中具有重要作用,本研究强调MØ和Treg细胞在HPV相关宫颈病变严重程度过程中的重要作用,提示它们可能作为预后标志物和免疫治疗靶点。
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来源期刊
CiteScore
2.60
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: Immunology covers a broad spectrum of investigations at the genes, molecular, cellular, organ and system levels to reveal defense mechanisms against pathogens as well as protection against tumors and autoimmune diseases. The great advances in immunology in recent years make this field one of the most dynamic and rapidly growing in medical sciences. Critical ReviewsTM in Immunology (CRI) seeks to present a balanced overview of contemporary adaptive and innate immune responses related to autoimmunity, tumor, microbe, transplantation, neuroimmunology, immune regulation and immunotherapy from basic to translational aspects in health and disease. The articles that appear in CRI are mostly obtained by invitations to active investigators. But the journal will also consider proposals from the scientific community. Interested investigators should send their inquiries to the editor before submitting a manuscript.
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