Human cytomegalovirus (HCMV) long-term shedding and HCMV-specific immune response in pregnant women with primary HCMV infection.

IF 5.5 3区 医学 Q1 IMMUNOLOGY
Medical Microbiology and Immunology Pub Date : 2022-12-01 Epub Date: 2022-08-12 DOI:10.1007/s00430-022-00747-4
C Fornara, F Zavaglio, M Furione, A Sarasini, P d'Angelo, A Arossa, A Spinillo, D Lilleri, F Baldanti
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引用次数: 5

Abstract

Human cytomegalovirus (HCMV) shedding has been extensively investigated in newborns and in young children, however, much less is known about it in immunocompetent adults. Shedding of HCMV was investigated in saliva, vaginal secretions and urine of pregnant women experiencing primary infection along with the development of the HCMV-specific immune response. Thirty-three pregnant women shed HCMV DNA in peripheral biological fluids at least until one year after onset of infection, while in blood HCMV DNA was cleared earlier. Significantly higher levels of viral load were found in vaginal secretions compared to saliva and urine. All subjects examined two years after the onset of infection showed a high avidity index, with IgM persisting in 36% of women. Viral load in blood was directly correlated with levels of HCMV-specific IgM and inversely correlated with levels of IgG specific for the pentameric complex gH/gL/pUL128L; in addition, viral load in blood was inversely correlated with percentage of HCMV-specific CD4+ and CD8+ expressing IL-7R (long-term memory, LTM) while viral load in biological fluids was inversely correlated with percentage of HCMV-specific CD4+ and CD8+ effector memory RA+(TEMRA). In conclusion, viral shedding during primary infection in pregnancy persists in peripheral biological fluids for at least one year and the development of both antibodies (including those directed toward the pentameric complex) and memory T cells are associated with viral clearance.

Abstract Image

人巨细胞病毒(HCMV)在原发性HCMV感染孕妇中的长期脱落和HCMV特异性免疫反应
人类巨细胞病毒(HCMV)的脱落已经在新生儿和幼儿中进行了广泛的研究,然而,在免疫能力强的成年人中却知之甚少。随着HCMV特异性免疫反应的发展,研究了原发性感染孕妇的唾液、阴道分泌物和尿液中HCMV的脱落情况。33名孕妇外周血中HCMV DNA至少在感染开始一年后才脱落,而血液中HCMV DNA更早被清除。与唾液和尿液相比,阴道分泌物中的病毒载量明显更高。在感染发生两年后进行检查的所有受试者都显示出较高的贪婪指数,36%的女性持续存在IgM。血中病毒载量与hcmv特异性IgM水平直接相关,与五聚体复合物gH/gL/pUL128L特异性IgG水平负相关;此外,血液中的病毒载量与表达IL-7R的hcmv特异性CD4+和CD8+百分比(长期记忆,LTM)呈负相关,而生物体液中的病毒载量与hcmv特异性CD4+和CD8+效应记忆RA+百分比(TEMRA)呈负相关。综上所述,妊娠期初次感染期间的病毒脱落在外周血液中持续至少一年,抗体(包括针对五聚体复合物的抗体)和记忆T细胞的产生与病毒清除有关。
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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
29
审稿时长
1 months
期刊介绍: Medical Microbiology and Immunology (MMIM) publishes key findings on all aspects of the interrelationship between infectious agents and the immune system of their hosts. The journal´s main focus is original research work on intrinsic, innate or adaptive immune responses to viral, bacterial, fungal and parasitic (protozoan and helminthic) infections and on the virulence of the respective infectious pathogens. MMIM covers basic, translational as well as clinical research in infectious diseases and infectious disease immunology. Basic research using cell cultures, organoid, and animal models are welcome, provided that the models have a clinical correlate and address a relevant medical question. The journal also considers manuscripts on the epidemiology of infectious diseases, including the emergence and epidemic spreading of pathogens and the development of resistance to anti-infective therapies, and on novel vaccines and other innovative measurements of prevention. The following categories of manuscripts will not be considered for publication in MMIM: submissions of preliminary work, of merely descriptive data sets without investigation of mechanisms or of limited global interest, manuscripts on existing or novel anti-infective compounds, which focus on pharmaceutical or pharmacological aspects of the drugs, manuscripts on existing or modified vaccines, unless they report on experimental or clinical efficacy studies or provide new immunological information on their mode of action, manuscripts on the diagnostics of infectious diseases, unless they offer a novel concept to solve a pending diagnostic problem, case reports or case series, unless they are embedded in a study that focuses on the anti-infectious immune response and/or on the virulence of a pathogen.
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