Author summary Oral cholera vaccines (OCV) are now on the WHO stockpile and targeted for use for countries with outbreaks and epidemics but also for control of endemic cholera. In Bangladesh many studies have been carried out to assess the safety, immunogenicity as well as feasibility of vaccination in the endemic settings of the country. However, with the large recent influx of displaced Rohingya nationals from Myanmar (termed Forcibly Displace Myanmar National; FDMN), mass campaigns with OCV were conducted between October 2017-December 2018. However, no data is available of the previous exposure to cholera of this population, prior to their arrival in Bangladesh. An assessment of immunogenicity status of FDMN is needed to find out if OCV is able to elicit comparable immune response and whether the same dose regimen of OCV was immunogenic among the FDMNs. In this study, we have measured the immune responses to the OCV, Shanchol, in adults (18 years and above), older children (6-17 years), and younger children (1-5 years). The results of this study shows that the oral cholera vaccine capable of inducing an immune response in adults and children among this FDMN population and the responses were comparable to that seen in Bangladeshi participants in earlier studies. After the large influx of Rohingya nationals (termed Forcibly Displaced Myanmar National; FDMN) from Rakhine State of Myanmar to Cox's Bazar in Bangladesh, it was apparent that outbreaks of cholera was very likely in this setting where people were living under adverse water and sanitation conditions. Large campaigns of oral cholera vaccine (OCV) were carried out as a preemptive measure to control cholera epidemics. The aim of the study was to evaluate the immune responses of healthy adults and children after administration of two doses of OCV at 14 days interval in FDMN population and compare with the response observed in Bangladeshi's vaccinated earlier. A cross-sectional immunogenicity study was conducted among FDMNs of three age cohort; in adults (18+years; n = 83), in older children (6-17 years; n = 63) and in younger children (1-5 years; n = 80). Capillary blood was collected at three time points to measure vibriocidal antibodies using either plasma or dried blood spot (DBS) specimens. There was a significant increase of responder frequency of vibriocidal antibody titer at day 14 in all groups for Vibrio cholerae O1 (Ogawa/Inaba: adults-64%/64%, older children-70%/89% and younger children-51%/75%). There was no overall difference of vibriocidal antibody titer between FDMN and Bangladeshi population at baseline (p = 0.07-0.08) and at day 14, day 28 in all age groups for both serotypes. The seroconversion rate and geometric mean titer (GMT) of either serotype were comparable using both plasma and DBS specimens. These results showed that OCV is capable of inducing robust immune responses in adults and children among the FDMN population which is comparable to that seen in Bangladeshi participants in different age groups or that reported from other cholera endemic countries. Our results also suggest that the displaced population were exposed to V. cholerae prior to seeking shelter in Bangladesh.
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ACTED Faim AAMACL International C Aid C NGOs CoD Council DR, 2018, ON YEAR MEAN PROGR N
机构:Int Ctr Diarrhoeal Dis Res, Div Sci Lab, Immunol Unit, Dhaka 1212, Bangladesh
Alam, Mohammad Murshid
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Riyadh, M. Asrafuzzaman
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Calderwood, Stephen B.
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Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Harvard Univ, Sch Med, Dept Med, Boston, MA USA
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Calderwood, Stephen B.
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Harris, Jason B.
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Ryan, Edward T.
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Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
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Charles, Richelle C.
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Hilaire, Isabelle J.
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Jerome, J. Gregory
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Saha, Amit
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Yu, Yanan
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NIDDKD, Bioorgan Chem Lab, NIH, Bethesda, MD USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
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Calderwood, Stephen B.
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Ryan, Edward T.
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LaRocque, Regina C.
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Ivers, Louise C.
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Harris, Jason B.
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Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
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Massachusetts Gen Hosp, Boston, MA 02114 USA
Harvard Univ, Sch Med, Boston, MA USA
Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USAInt Ctr Diarrhoeal Dis Res, Div Sci Lab, Dhaka 1000, Bangladesh
机构:Int Ctr Diarrhoeal Dis Res, Div Sci Lab, Immunol Unit, Dhaka 1212, Bangladesh
Alam, Mohammad Murshid
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Riyadh, M. Asrafuzzaman
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Fatema, Kaniz
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Calderwood, Stephen B.
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Harvard Univ, Sch Med, Dept Med, Boston, MA USA
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Harris, Jason B.
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Ryan, Edward T.
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Qadri, Firdausi
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Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Harvard Univ, Sch Med, Dept Med, Boston, MA USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Charles, Richelle C.
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Hilaire, Isabelle J.
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Partners Hlth, Boston, MA USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Hilaire, Isabelle J.
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Mayo-Smith, Leslie M.
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Teng, Jessica E.
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Brigham & Womens Hosp, Div Global Hlth Equ, Boston, MA 02115 USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Teng, Jessica E.
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Jerome, J. Gregory
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Jerome, J. Gregory
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Franke, Molly F.
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Partners Hlth, Boston, MA USA
Harvard Univ, Sch Med, Dept Global Hlth & Social Med, Boston, MA USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Franke, Molly F.
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Saha, Amit
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Icddr B, Dhaka, BangladeshMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Saha, Amit
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Yu, Yanan
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Yu, Yanan
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Kovac, Paul
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NIDDKD, Bioorgan Chem Lab, NIH, Bethesda, MD USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Kovac, Paul
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Calderwood, Stephen B.
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Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Harvard Univ, Sch Med, Dept Med, Boston, MA USA
Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Boston, MA USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Calderwood, Stephen B.
;
Ryan, Edward T.
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Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Harvard Univ, Sch Med, Dept Med, Boston, MA USA
Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Ryan, Edward T.
;
LaRocque, Regina C.
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Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Harvard Univ, Sch Med, Dept Med, Boston, MA USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
LaRocque, Regina C.
;
Almazor, Charles P.
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Partners Hlth, Boston, MA USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Almazor, Charles P.
;
Qadri, Firdausi
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Icddr B, Dhaka, BangladeshMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Qadri, Firdausi
;
Ivers, Louise C.
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Harvard Univ, Sch Med, Dept Med, Boston, MA USA
Partners Hlth, Boston, MA USA
Brigham & Womens Hosp, Div Global Hlth Equ, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Global Hlth & Social Med, Boston, MA USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Ivers, Louise C.
;
Harris, Jason B.
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h-index: 0
机构:
Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USAMassachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
机构:
Massachusetts Gen Hosp, Boston, MA 02114 USA
Harvard Univ, Sch Med, Boston, MA USA
Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USAInt Ctr Diarrhoeal Dis Res, Div Sci Lab, Dhaka 1000, Bangladesh