학술논문

Analysis of Humoral Immune Responses in Chikungunya Virus (CHIKV)-Infected Patients and Individuals Vaccinated With a Candidate CHIKV Vaccine.
Document Type
Journal Article
Source
Journal of Infectious Diseases. 5/15/2020, Vol. 221 Issue 10, p1713-1723. 11p.
Subject
*HUMORAL immunity
*CHIKUNGUNYA virus
*ALPHAVIRUSES
*ALPHAVIRUS diseases
*VACCINES
*VACCINE effectiveness
*COMPARATIVE studies
*EPITHELIAL cells
*GENES
*IMMUNITY
*IMMUNIZATION
*IMMUNOGLOBULINS
*IMMUNOLOGY technique
*RESEARCH methodology
*MEDICAL cooperation
*MOLECULAR structure
*RESEARCH
*VIRAL antibodies
*VIRAL vaccines
*PROTEOMICS
*EVALUATION research
*CHIKUNGUNYA
*ANTIBODY formation
Language
ISSN
0022-1899
Abstract
Background: Chikungunya virus (CHIKV) is a mosquito-transmitted alphavirus that causes severe flu-like symptoms. The acute symptoms disappear after 1 week, but chronic arthralgia can persist for years. In this study, humoral immune responses in CHIKV-infected patients and vaccinees were analyzed.Methods: Alphavirus neutralization activity was analyzed with pseudotyped lentiviral vectors, and antibody epitope mapping was performed with a peptide array.Results: The greatest CHIKV neutralization activity was observed 60-92 days after onset of symptoms. The amount of CHIKV-specific antibodies and their binding avidity and cross-reactivity with other alphaviruses increased over time. Chikungunya virus and o'nyong-nyong virus (ONNV) were both neutralized to a similar extent. Linear antibody binding epitopes were mainly found in E2 domain B and the acid-sensitive regions (ASRs). In addition, serum samples from healthy volunteers vaccinated with a measles-vectored chikungunya vaccine candidate, MV-CHIK, were analyzed. Neutralization activity in the samples from the vaccine cohort was 2- to 6-fold lower than in samples from CHIKV-infected patients. In contrast to infection, vaccination only induced cross-neutralization with ONNV, and the E2 ASR1 was the major antibody target.Conclusions: These data could assist vaccine design and enable the identification of correlates of protection necessary for vaccine efficacy. [ABSTRACT FROM AUTHOR]