Immune Parameters in the Cord Blood of Newborns Exposed to Malaria in the Womb

Sponsor
National Institute of Allergy and Infectious Diseases (NIAID) (NIH)
Overall Status
Completed
CT.gov ID
NCT00772642
Collaborator
(none)
120
1
23.1
5.2

Study Details

Study Description

Brief Summary

This study, conducted by the Malaria Research and Training Center at the University of Bamako, Mali, and the NIAID, will examine how exposure to the malaria parasite in the womb affects the developing immune system of newborns. Little is known about how such exposure in the womb may affect the immune system or alter the risk of malaria or responsiveness to vaccination after birth. A better understanding of this process may provide information useful for childhood vaccination strategies in areas where malaria is widespread.

Women 18 years of age and older who live in Bancoumana and are in their last trimester of pregnancy and in good health may be eligible for this study.

Participants have blood samples drawn from a finger stick and through a needle placed in a vein two times for this study: when they enroll in the study and again when they go to the Bancoumana Health Center to deliver their baby. After the baby and placenta are delivered, blood is collected from the umbilical cord and placenta.

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Condition or Disease Intervention/Treatment Phase

    Detailed Description

    In malaria endemic areas the fetus is at risk for in utero exposure to Plasmodium falciparum or its soluble products. Little is known about how this exposure modulates the developing fetal immune system, or how this may alter the risk of malaria or responsiveness to vaccination after birth. A clearer understanding of this process may inform childhood vaccination strategies in malaria endemic areas. The objective of this cross-sectional exploratory study is to define the immune profile associated with in utero exposure to P. falciparum by analyzing cord blood samples collected at a site of high malaria transmission in Mali, and to compare this profile to that of U.S. cord blood samples. Pregnant women will be invited to participate in this study during the 3rd trimester of pregnancy. A finger stick blood draw will be collected from the mother at enrollment and peri-partum to determine if she is infected with P. falciparum. Cord blood and placental blood samples will be collected post-partum and processed to obtain mononuclear cells and serum. Cord blood can be obtained from the placenta after delivery without risk to mother or infant and will be used for research purposes only. Mononuclear cells will be analyzed by flow cytometry to characterize subsets of B, T and innate immune cells. Functional assays such as the B and T cell ELISPOT assay and measurements of cytokines in response to in vitro stimulation will also be performed.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    120 participants
    Time Perspective:
    Other
    Official Title:
    Profiling Immunological Parameters in the Cord Blood of Neonates Exposed to Plasmodium Falciparum in Utero
    Study Start Date :
    Oct 8, 2008
    Study Completion Date :
    Sep 10, 2010

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years to 99 Years
      Sexes Eligible for Study:
      Female
      Accepts Healthy Volunteers:
      No
      • INCLUSION CRITERIA:

      • Age greater than or equal to 18 years

      • Healthy female in 3rd trimester of pregnancy

      • Resident of Bancoumana

      • Willingness to allow cord and placental blood samples to be stored and used for future studies of the immune response to malaria

      • Ability to give informed consent and willingness to comply with study requirements and procedures

      EXCLUSION CRITERIA:
      • Currently taking corticosteroids or other immunosuppressants

      • Underlying heart disease, bleeding disorder, or other condition that in the judgment of the Principal Investigator (PI) could increase the risk to the volunteer

      • Fever greater than or equal to 37.5 degree C or evidence of an acute infection

      • Anemia (hemoglobin less than 9 g/dL)

      • Participation in another clinical protocol that requires the administration of an experimental vaccine or experimental treatment.

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Malaria Research and Training Center Bamako Mali

      Sponsors and Collaborators

      • National Institute of Allergy and Infectious Diseases (NIAID)

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00772642
      Other Study ID Numbers:
      • 999909004
      • 09-I-N004
      First Posted:
      Oct 15, 2008
      Last Update Posted:
      Jul 2, 2017
      Last Verified:
      Sep 10, 2010
      Keywords provided by , ,
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Jul 2, 2017