Sustained Long-Term Decline in Anti-HCV Neutralizing Antibodies in HIV/HCV-Coinfected Patients Five Years after HCV Therapy: A Retrospective Study
<b>Background:</b> This study evaluated titers and amplitudes of anti-E2 antibodies (anti-E2-Abs) and neutralizing antibodies against hepatitis C virus (HCV; anti-HCV-nAbs) in HIV/HCV-coinfected individuals over five years after successful HCV treatment completion. <b>Methods:</b> We retrospectively analyzed 76 HIV/HCV-coinfected patients achieving sustained virologic response post-HCV treatment. Plasma levels of anti-E2-Abs and anti-HCV-nAbs against five HCV genotypes (Gt1a, Gt1b, Gt2a, Gt3a, and Gt4a) were determined using ELISA and microneutralization assays, respectively. Statistical analyses comparing the three follow-up time points (baseline, one year, and five years post-HCV treatment) were performed using generalized linear mixed models, adjusting <i>p</i>-values with the false discovery rate (<i>q</i>-value). <b>Results:</b> Compared to baseline, anti-E2-Abs titers decreased at one year (1.9- to 2.3-fold, <i>q</i>-value < 0.001) and five years (3.4- to 9.1-fold, <i>q</i>-value < 0.001) post-HCV treatment. Anti-HCV-nAbs decreased 2.9- to 8.4-fold (<i>q</i>-value < 0.002) at one year and 17.8- to 90.4-fold (<i>q</i>-value < 0.001) at five years post-HCV treatment. Anti-HCV-nAbs titers against Gt3a were consistently the lowest. Nonresponse rates for anti-E2-Abs remained low throughout the follow-up, while anti-HCV-nAbs nonresponse rates increased 1.8- to 13.5-fold (<i>q</i>-value < 0.05) at five years post-HCV treatment, with Gt3a showing the highest nonresponse rate. <b>Conclusions:</b> Humoral immune responses against HCV decreased consistently one and five years post-HCV treatment, regardless of HCV genotype and previous HCV therapy or type of treatment (IFN- or DAA-based therapy). This decline was more pronounced for anti-HCV-nAbs, particularly against Gt3.
Authors
- Rubén Martín‐Escolano (ORCID: https://orcid.org/0000-0002-6262-9344)
- Salvador Resino (ORCID: https://orcid.org/0000-0001-8783-0450)
- Víctor Hontañón (ORCID: https://orcid.org/0000-0003-3070-2647)
- Juan Berenguer (ORCID: https://orcid.org/0000-0001-8541-8200)
- Rafael Amigot‐Sánchez (ORCID: https://orcid.org/0000-0001-9253-1631)
- Isidoro Martínez (ORCID: https://orcid.org/0000-0002-9949-9264)
- Julián Gómez‐Gutiérrez (ORCID: https://orcid.org/0000-0002-1653-6673)
- Belén Yélamos (ORCID: https://orcid.org/0000-0002-0559-0367)
- Cristina Díez (ORCID: https://orcid.org/0000-0002-3508-9979)
- Daniel Sepúlveda‐Crespo (ORCID: https://orcid.org/0000-0002-8053-6045)
- Juan González‐García (ORCID: https://orcid.org/0000-0002-3652-002X)
- Camilla Volpi
Institutions
- Universidad Complutense de Madrid (ES)
- University of Milan (IT)
- Hospital Universitario La Paz (ES)
- Instituto de Salud Carlos III (ES)
- Hospital General Universitario Gregorio Marañón (ES)
- Centro Nacional de Microbiologia (ES)
- Centro de Investigación Biomédica en Red (ES)
Publication Details
- Journal
- Pharmaceuticals
- Published
- 2024-08-30
- DOI
- https://doi.org/10.3390/ph17091152
- Citations
- 2
- Primary Topic
- Hepatitis C virus research
- Type
- article
- Field-Weighted Citation Impact
- 0.74
Funders
- Sociedad Española de Enfermedades Infecciosas y Microbiología Clínica
- Instituto de Salud Carlos III