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A Noninvasive Method to Sample Immune Cells in the Lower Female Genital Tract Using Menstrual Discs.
Peters, M Quinn; Domenjo-Vila, Eva; Carlson, Marc; Armistead, Blair; Edlefsen, Paul T; Gasper, Melanie; Dabee, Smritee; Whidbey, Christopher; Jaspan, Heather B; Prlic, Martin; Harrington, Whitney E.
Afiliación
  • Peters MQ; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.
  • Domenjo-Vila E; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Carlson M; Research Scientific Computing, Enterprise Analytics, Seattle Children's Research Institute, Seattle, WA.
  • Armistead B; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.
  • Edlefsen PT; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Gasper M; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.
  • Dabee S; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.
  • Whidbey C; Department of Chemistry, Seattle University, Seattle, WA.
  • Jaspan HB; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.
  • Prlic M; Department of Pediatrics, University of Washington, Seattle, WA.
  • Harrington WE; Department of Global Health, University of Washington, Seattle, WA.
Immunohorizons ; 8(2): 182-192, 2024 Feb 01.
Article en En | MEDLINE | ID: mdl-38386594
ABSTRACT
T cells in the human female genital tract (FGT) are key mediators of susceptibility to and protection from infection, including HIV and other sexually transmitted infections. There is a critical need for increased understanding of the distribution and activation of T cell populations in the FGT, but current sampling methods require a healthcare provider and are expensive, limiting the ability to study these populations longitudinally. To address these challenges, we have developed a method to sample immune cells from the FGT utilizing disposable menstrual discs which are noninvasive, self-applied, and low in cost. To demonstrate reproducibility, we sampled the cervicovaginal fluid of healthy, reproductive-aged individuals using menstrual discs across 3 sequential days. Cervicovaginal fluid was processed for cervicovaginal cells, and high-parameter flow cytometry was used to characterize immune populations. We identified large numbers of live, CD45+ leukocytes, as well as distinct populations of T cells and B cells. Within the T cell compartment, activation and suppression status of T cell subsets were consistent with previous studies of the FGT utilizing current approaches, including identification of both tissue-resident and migratory populations. In addition, the T cell population structure was highly conserved across days within individuals but divergent across individuals. Our approach to sample immune cells in the FGT with menstrual discs will decrease barriers to participation and empower longitudinal sampling in future research studies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones por VIH Límite: Adult / Female / Humans Idioma: En Revista: Immunohorizons Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones por VIH Límite: Adult / Female / Humans Idioma: En Revista: Immunohorizons Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos