The objective of this study was to evaluate the association of the human leukocyte antigen (HLA) class II genes , and with the humoral immune response elicited by inactivated Japanese encephalitis (JE) vaccine (IJEV). A total of 373 individuals aged 3-12 years in the Inner Mongolia Autonomous Region in China, who received two doses of IJEV at 0 and 7 days, were enrolled in the current study. Based on the individuals' specific JE virus (JEV)-neutralizing antibodies (NAbs), they were divided into a seropositive and a seronegative group. , and were genotyped using a sequencing-based typing method. Next, the association of the HLA class II genes and their haplotypes with antibody response was evaluated. Based on NAbs, a total of 161 individuals were classified as seropositive and 212 as seronegative. was significantly associated with JEV seropositivity ( < 0.001, OR = 0.364, 95% CI: 0.221-0.600), while was significantly associated with JEV seronegativity ( = 5.03 × 10, OR = 7.341, 95% CI: 2.876-18.736). The haplotypes , and were very frequent in the seropositive group, while , and were very frequent in the seronegative group. The presence of , and was associated with a higher geometric mean titer (GMT) of NAbs than that of at the locus ( < 0.05). At the locus, the presence of was associated with higher GMTs than that of and ( < 0.05), and the presence of and was associated with higher GMTs than that of ( < 0.05). The present study suggests that HLA class II genes may influence the antibody response to IJEV.
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http://dx.doi.org/10.3389/fimmu.2019.00428 | DOI Listing |
Int J Mol Sci
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Immunology Department, University Hospital Marqués de Valdecilla, 39008 Santander, Spain.
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State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, 300020, China.
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February 2025
GROW Research Institute for Oncology and Reproduction, Maastricht University, Maastricht, The Netherlands.
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View Article and Find Full Text PDFVaccines (Basel)
January 2025
The GWI and HLA Research Groups, Brain Sciences Center, Department of Veterans Affairs Health Care System, Minneapolis, MN 55417, USA.
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View Article and Find Full Text PDFVaccines (Basel)
January 2025
The Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford OX3 7DQ, UK.
After four decades of intensive research, traditional vaccination strategies for HIV-1 remain ineffective due to HIV-1's extraordinary genetic diversity and complex immune evasion mechanisms. Cytomegaloviruses (CMV) have emerged as a novel type of vaccine vector with unique advantages due to CMV persistence and immunogenicity. Rhesus macaques vaccinated with molecular clone 68-1 of RhCMV (RhCMV68-1) engineered to express simian immunodeficiency virus (SIV) immunogens elicited an unconventional major histocompatibility complex class Ib allele E (MHC-E)-restricted CD8 T-cell response, which consistently protected over half of the animals against a highly pathogenic SIV challenge.
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