Characterisation of human antibody responses to Chikungunya virus infection / Chua Chong Long
Chikungunya virus (CHIKV), an alphavirus of the family Togaviridae, causes fever, rash and joint pain. There are three CHIKV genotypes: West African, Asian and East/Central/South African (ECSA). The latter two genotypes have been co-circulating and causing outbreaks in Malaysia. Although vaccines...
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| Format: | Thesis |
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2017
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| Online Access: | http://studentsrepo.um.edu.my/10358/4/chong_long.pdf http://studentsrepo.um.edu.my/10358/ |
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| Summary: | Chikungunya virus (CHIKV), an alphavirus of the family Togaviridae, causes fever,
rash and joint pain. There are three CHIKV genotypes: West African, Asian and
East/Central/South African (ECSA). The latter two genotypes have been co-circulating
and causing outbreaks in Malaysia. Although vaccines are still under development, a
greater understanding of the human antibody responses to CHIKV infection is essential.
The overall aim of the present study was to characterise human antibody responses to
CHIKV. The antibody responses were studied in 102 serum samples collected during
CHIKV outbreaks in Malaysia. The first objective of the study was to develop a panel
of monoclonal antibodies targeting CHIKV E2 glycoprotein as immunological tools.
The monoclonal antibody clone B-D2(C4) was chosen for use in subsequent serum
neutralisation assay and development of immunoassays. For the second objective, the
characteristics of cross-genotype immunity and epitopes were investigated. The
neutralising capacity of late convalescent sera (ECSA and Asian) was analysed against
representative clinical isolates as well as viruses rescued from infectious clones of
ECSA and Asian CHIKV. Using whole virus antigen and recombinant E1 and E2
envelope glycoproteins, the antibody binding sites, epitopes and antibody titres were
investigated using ELISA and western blotting. Both ECSA and Asian sera
demonstrated stronger neutralising capacity against ECSA genotype, which corresponds
to stronger epitope-antibody interaction. ECSA serum targeted conformational epitope
sites in the E1-E2 glycoprotein, while E1-E211K, E2-I2T, E2-H5N, E2-G118S and E2-
S194G were the key amino acids that enhanced cross-neutralising efficacy. As for Asian
serum, the antibodies targeting E2 glycoprotein correlated with neutralising efficacy and
I2T, H5N, G118S and S194G altered and improved the neutralisation efficacy. For the
third objective, the pathogenic role of antibodies from immune sera was explored.
Evidence for CHIKV antibody-dependent enhancement (ADE) was demonstrated in
iv
K562 leukaemia cells, which express the Fc gamma receptor FcɣRIIA (CD32) and
supports active virus production. For the fourth objective, the neutralising role of IgM at
different times post-infection was described and the independent contributions of IgM
and IgG towards the neutralising capacity of human immune sera were examined. The
differences in neutralising epitopes of IgM and IgG were investigated as well.
Neutralising IgM starts to appear as early as day 4 of symptoms, and their appearance
from day 6 is associated with a reduction in viraemia. IgM acts in a complementary
manner with early IgG, but plays the main neutralising role up to a point between days 4
and 10 which varies between individuals. After this point, total neutralising capacity is
attributable almost entirely to the robust neutralising IgG response. IgM preferentially
binds and targets epitopes on the CHIKV surface E1-E2 glycoproteins, rather than
individual E1 or E2. Overall, the findings from this study provide new knowledge in the
immunoprotection mechanisms against co-circulating CHIKV genotypes. The findings
have implications for effective design and development of vaccines, human monoclonal
antibodies and diagnostic serological assays. |
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