Evaluation of the In Vitro Capacity of Anti-Human Cytomegalovirus Antibodies to Initiate Antibody-Dependent Cell Cytotoxicity

Bibliographic Details
Title: Evaluation of the In Vitro Capacity of Anti-Human Cytomegalovirus Antibodies to Initiate Antibody-Dependent Cell Cytotoxicity
Authors: Piera d’Angelo, Federica Zavaglio, Elisa Gabanti, Paola Zelini, Chiara Fornara, Stefano Bernuzzi, Arsenio Spinillo, Daniele Lilleri, Fausto Baldanti
Source: Microorganisms, Vol 12, Iss 7, p 1355 (2024)
Publisher Information: MDPI AG, 2024.
Publication Year: 2024
Collection: LCC:Biology (General)
Subject Terms: herpesviruses, human cytomegalovirus (HCMV), NK cells, antibodies, non-neutralizing antibodies, antibody-dependent cell cytotoxicity (ADCC), Biology (General), QH301-705.5
More Details: In the setting of infectious diseases, antibodies show different functions beyond neutralizing activity. In this study, we investigated the activation of NK cells in vitro in the presence of human cytomegalovirus (HCMV)-specific antibodies and their potential role in the control of HCMV infection through antibody-dependent cell cytotoxicity (ADCC). Retinal pigmented epithelial cells (ARPE-19) infected with the HCMV strain VR1814 were co-cultured with cytokine-activated peripheral blood mononuclear cells (PBMCs) in the presence of sera collected from 23 HCMV-seropositive and 9 HCMV-seronegative donors. Moreover, 13 pregnant women sampled 3 and 6 months after HCMV primary infection and 13 pregnant women with pre-conception immunity were tested and compared. We determined the percentage of activated NK cells via the analysis of CD107a expression as a marker of degranulation. Significantly higher levels of NK-cell activation were observed using 1/100 and 1/10 dilutions of sera from HCMV-seropositive individuals, and when cells were infected for 96 and 120 h, suggesting that NK cells are activated by antibodies directed against late antigens. In the absence of serum NK cells, activation was negligible. In seropositive subjects, the median percentages of CD107a-positive NK cells in the presence of autologous serum and pooled HCMV-positive serum were similar (14.03% [range 0.00–33.56] and 12.42% [range 1.01–46.00], respectively), while NK-cell activation was negligible using an HCMV-negative serum pool. In HCMV-seronegative subjects, the median percentage of activated NK cells was 0.90% [range 0.00–3.92] with autologous serum and 2.07% [0.00–5.76] in the presence of the HCMV-negative serum pool, while it was 8.97% [0.00–26.49] with the pool of HCMV-positive sera. NK-cell activation using hyperimmune globulin is comparable to what is obtained using autologous serum. Sera from subjects at 3 and 6 months post primary infection showed a lower capacity of NK-cell activation than sera from subjects with past infection (p < 0.001). NK activation against HCMV-infected epithelial cells is dependent on the presence of HCMV-specific antibodies. This serum activity increases with time after the onset of HCMV infection. The protective role of NK-cell activation by HCMV-specific serum antibodies should be verified in clinical settings.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2076-2607
Relation: https://www.mdpi.com/2076-2607/12/7/1355; https://doaj.org/toc/2076-2607
DOI: 10.3390/microorganisms12071355
Access URL: https://doaj.org/article/86b5b96bb15447f78517d133744b4b92
Accession Number: edsdoj.86b5b96bb15447f78517d133744b4b92
Database: Directory of Open Access Journals
More Details
ISSN:20762607
DOI:10.3390/microorganisms12071355
Published in:Microorganisms
Language:English