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Novel sporozoite-based ELISpot assay to assess frequency of parasite-specific B cells after vaccination with irradiated sporozoites.
Atre, Tanmaya; Robinson, Tanisha M; Savransky, Tatyana; Dutta, Sheetij; Epstein, Judith E; Bergmann-Leitner, Elke S.
Affiliation
  • Atre T; Malaria Vaccine Branch, US Military Malaria Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
  • Robinson TM; Malaria Vaccine Branch, US Military Malaria Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
  • Savransky T; Division of Entomology, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
  • Dutta S; Malaria Vaccine Branch, US Military Malaria Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
  • Epstein JE; Malaria Department, Naval Medical Research Center, Silver Spring, MD, USA.
  • Bergmann-Leitner ES; Malaria Vaccine Branch, US Military Malaria Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, USA. elke.s.bergmann-leitner.civ@mail.mil.
Malar J ; 18(1): 186, 2019 May 29.
Article in En | MEDLINE | ID: mdl-31142328
BACKGROUND: Whole parasite vaccination is an efficacious strategy to induce sterile immunity and to prevent malaria transmission. Understanding the mechanism and response of immune cells to vaccines plays a critical role in deciphering correlates of protection against infection and disease. Immunoassays, such as ELISpot, are commonly used to assess the immunogenicity of vaccines towards T cells and B cells. To date, these assays only analyse responses to specific antigens since they are based on recombinant parasite-derived proteins or peptides. There is the need for an agnostic approach that allows the evaluation of all sporozoite-associated antigens. METHODS: ELISpot plates coated with a defined amount of lysed Plasmodium falciparum sporozoites were used to assess the frequency of sporozoite-specific B cells in peripheral blood mononuclear cells from donors immunized with either a recombinant malaria vaccine or irradiated sporozoites. RESULTS: This report describes the assay conditions for a specific and sensitive sporozoite-based B cell ELISpot assay. The assay development considers the quality of sporozoite preparation as well as the detection threshold of the frequency of antigen-specific B cells. The assay enables the detection of sporozoite-specific IgM and IgG-producing B cells. Moreover, the assay can detect sporozoite-reactive B cells from subjects that were either vaccinated with the radiation attenuated sporozoite vaccine or a recombinant pre-erythrocytic vaccine. CONCLUSION: The newly developed sporozoite-based B cell ELISpot enables the monitoring of changes in the frequency of sporozoite-specific B cells. Applying this assay to assess the potency of vaccination regimens or seasonal changes in B cell populations from subjects residing in malaria-endemic areas will provide an opportunity to gain insight into immune mechanisms involved in protection and/or disease.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: B-Lymphocytes / Malaria Vaccines / Sporozoites / Enzyme-Linked Immunospot Assay Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Malar J Journal subject: MEDICINA TROPICAL Year: 2019 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: B-Lymphocytes / Malaria Vaccines / Sporozoites / Enzyme-Linked Immunospot Assay Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Malar J Journal subject: MEDICINA TROPICAL Year: 2019 Document type: Article Affiliation country: United States Country of publication: United kingdom