TY - JOUR
T1 - Antibody profiles to plasmodium merozoite surface protein-1 in Cambodian adults during an active surveillance cohort with nested treatment study
AU - Spring, Michele D.
AU - Pichyangkul, Sathit
AU - Lon, Chanthap
AU - Gosi, Panita
AU - Yongvanichit, Kosol
AU - Srichairatanakul, Utaiwan
AU - Limsalakpeth, Amporn
AU - Chaisatit, Chaiyaporn
AU - Chann, Soklyda
AU - Sriwichai, Sabaithip
AU - Auayapon, Montida
AU - Chaorattanakawee, Suwanna
AU - Dutta, Sheetij
AU - Prom, Satharath
AU - Meng Chour, Char
AU - Walsh, Douglas S.
AU - Angov, Evelina
AU - Saunders, David L.
N1 - Publisher Copyright:
© 2016 Spring et al.
PY - 2016/1/8
Y1 - 2016/1/8
N2 - Background: In addition to evidence for a protective role of antibodies to the malaria blood stage antigen merozoite surface protein 1 (MSP1), MSP1 antibodies are also considered as a marker of past malaria exposure in sero-epidemiological studies. Methods: In order to better assess the potential use of MSP1 serology in malaria chemoprophylaxis trials in endemic areas, an analysis for the prevalence of antibodies to both Plasmodium falciparum and Plasmodium vivax MSP142 in healthy Cambodian adults was conducted at two sites as part of an active, observational cohort evaluating the efficacy of dihydroartemisinin-piperaquine (DP) for uncomplicated malaria (ClinicalTrials.gov identifier NCT01280162). Results: Rates of baseline sero-positivity were high (59 and 73 % for PfMSP142 and PvMSP142, respectively), and titers higher in those who lived in a higher transmission area, although there was little correlation in titers between the two species. Those volunteers who subsequently went on to develop malaria had higher baseline MSP142 titers than those who did not for both species. Titers to both antigens remained largely stable over the course of the 4-6 month study, except in those infected with P. falciparum who had multiple recurrences. Conclusion: These findings illuminate the difficulties in using MSP142 serology as either a screening criterion and/or biomarker of exposure in chemoprophylaxis studies. Further work remains to identify useful markers of malarial infection and/or immunity.
AB - Background: In addition to evidence for a protective role of antibodies to the malaria blood stage antigen merozoite surface protein 1 (MSP1), MSP1 antibodies are also considered as a marker of past malaria exposure in sero-epidemiological studies. Methods: In order to better assess the potential use of MSP1 serology in malaria chemoprophylaxis trials in endemic areas, an analysis for the prevalence of antibodies to both Plasmodium falciparum and Plasmodium vivax MSP142 in healthy Cambodian adults was conducted at two sites as part of an active, observational cohort evaluating the efficacy of dihydroartemisinin-piperaquine (DP) for uncomplicated malaria (ClinicalTrials.gov identifier NCT01280162). Results: Rates of baseline sero-positivity were high (59 and 73 % for PfMSP142 and PvMSP142, respectively), and titers higher in those who lived in a higher transmission area, although there was little correlation in titers between the two species. Those volunteers who subsequently went on to develop malaria had higher baseline MSP142 titers than those who did not for both species. Titers to both antigens remained largely stable over the course of the 4-6 month study, except in those infected with P. falciparum who had multiple recurrences. Conclusion: These findings illuminate the difficulties in using MSP142 serology as either a screening criterion and/or biomarker of exposure in chemoprophylaxis studies. Further work remains to identify useful markers of malarial infection and/or immunity.
KW - Antibodies
KW - Biomarker
KW - Chemoprophylaxis
KW - Malaria
KW - Merozoite surface protein 1
UR - http://www.scopus.com/inward/record.url?scp=84954122287&partnerID=8YFLogxK
U2 - 10.1186/s12936-015-1058-8
DO - 10.1186/s12936-015-1058-8
M3 - Article
C2 - 26747132
AN - SCOPUS:84954122287
SN - 1475-2875
VL - 15
JO - Malaria Journal
JF - Malaria Journal
IS - 1
M1 - 17
ER -