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Measles immunity gap among reproductive-age women participating in a simulated HIV vaccine efficacy trial in Zambia.
Malama, Kalonde; Tichacek, Amanda; Kelly, Hilary; Parker, Rachel; Inambao, Mubiana; Sharkey, Tyronza; Wall, Kristin M; Kilembe, William; Price, Matt A; Fast, Pat; Priddy, Fran; Allen, Susan.
Affiliation
  • Malama K; Center for Family Health Research in Zambia, Rwanda Zambia HIV Research Group, Lusaka, Zambia.
  • Tichacek A; Rwanda Zambia HIV Research Group, Emory University, School of Medicine, Atlanta, GA, USA.
  • Kelly H; Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Parker R; Rwanda Zambia HIV Research Group, Emory University, School of Medicine, Atlanta, GA, USA.
  • Inambao M; Center for Family Health Research in Zambia, Rwanda Zambia HIV Research Group, Ndola, Zambia.
  • Sharkey T; Center for Family Health Research in Zambia, Rwanda Zambia HIV Research Group, Lusaka, Zambia.
  • Wall KM; Rwanda Zambia HIV Research Group, Emory University, School of Medicine, Atlanta, GA, USA.
  • Kilembe W; Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA.
  • Price MA; Center for Family Health Research in Zambia, Rwanda Zambia HIV Research Group, Lusaka, Zambia.
  • Fast P; IAVI, New York, NY, USA.
  • Priddy F; Department of Epidemiology and Biostatistics, University of California at San Francisco, San Francisco, CA, USA.
  • Allen S; IAVI, New York, NY, USA.
Hum Vaccin Immunother ; 18(5): 2066426, 2022 11 30.
Article in En | MEDLINE | ID: mdl-35446726
ABSTRACT
Measles is a vaccine-preventable viral disease whose vaccination coverage remains low in Zambia, where the target group for vaccination is children aged 9 to 18 months. In addition to inadequate measles vaccination coverage among children, few studies address potential resultant immunity gaps among adults. We analyzed data from a simulated HIV vaccine efficacy trial (SiVET) conducted from 2015-2017 among adult Zambian women of childbearing age to determine measles antibody seroprevalence before and after vaccination with the measles, mumps and rubella (MMR) vaccine. We used MMR vaccine as a substitute for an experimental HIV vaccine as part of a simulation exercise to prepare for an HIV vaccine efficacy trial. We found that 75% of women had measles antibodies prior to receiving MMR, which increased to 98% after vaccination. In contrast, mumps and rubella antibody prevalence was high before (93% and 97%, respectively) and after (99% and 100%, respectively) vaccination. The low baseline measles seropositivity suggests an immunity gap among women of childbearing age. We recommend that measles vaccination programs target women of childbearing age, who can pass antibodies on to neonates. Moreover, administering the MMR vaccine to clinical trial candidates could prevent measles, mumps or rubella-related adverse events during actual trials.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rubella / HIV Infections / AIDS Vaccines / Vaccine-Preventable Diseases / Measles / Mumps Type of study: Clinical_trials / Risk_factors_studies Limits: Adult / Child / Female / Humans / Newborn Country/Region as subject: Africa Language: En Journal: Hum Vaccin Immunother Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rubella / HIV Infections / AIDS Vaccines / Vaccine-Preventable Diseases / Measles / Mumps Type of study: Clinical_trials / Risk_factors_studies Limits: Adult / Child / Female / Humans / Newborn Country/Region as subject: Africa Language: En Journal: Hum Vaccin Immunother Year: 2022 Document type: Article Affiliation country: