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Vaccine-related major cutaneous reaction size correlates with cellular-mediated immune responses after tularaemia immunisation.
Salerno-Gonçalves, Rosangela; Chen, Wilbur H; Mulligan, Mark J; Frey, Sharon E; Stapleton, Jack T; Keitel, Wendy A; Bailey, Jason; Sendra, Eli; Hill, Heather; Johnson, Robert A; Sztein, Marcelo B.
Afiliação
  • Salerno-Gonçalves R; Center for Vaccine Development and Global Health (CVD) University of Maryland School of Medicine Baltimore MD USA.
  • Chen WH; Center for Vaccine Development and Global Health (CVD) University of Maryland School of Medicine Baltimore MD USA.
  • Mulligan MJ; The Hope Clinic of the Emory Vaccine Center Department of Medicine Division of Infectious Diseases Emory University School of Medicine Decatur GA USA.
  • Frey SE; Present address: NYU Langone Vaccine Center NYU Grossman School of Medicine Alexandria Center for Life Sciences (West Tower) New York NY USA.
  • Stapleton JT; Division of Infectious Diseases, Allergy and Immunology Saint Louis University School of Medicine St. Louis MO USA.
  • Keitel WA; Iowa City Veterans Administration and the University of Iowa Iowa City IA USA.
  • Bailey J; Departments of Molecular Virology and Microbiology, and Medicine Baylor College of Medicine Houston TX USA.
  • Sendra E; Emmes Rockville MD USA.
  • Hill H; Present address: Armed Forces Health Surveillance Branch, Integrated Biosurveillance Silver Spring MD USA.
  • Johnson RA; Emmes Rockville MD USA.
  • Sztein MB; Emmes Rockville MD USA.
Clin Transl Immunology ; 10(1): e1239, 2021.
Article em En | MEDLINE | ID: mdl-33505681
ABSTRACT

OBJECTIVES:

Francisella tularensis, the causative agent of tularaemia, is an exceptionally infectious bacterium, potentially fatal for humans if left untreated and with the potential to be developed as a bioweapon. Both natural infection and live-attenuated vaccine strain (LVS) confer good protection against tularaemia. LVS vaccination is traditionally administered by scarification, and the formation of a cutaneous reaction or take at the vaccination site is recognised as a clinical correlate of protection. Although previous studies have suggested that high antibody titres following vaccination might serve as a useful surrogate marker, the immunological correlates of protection remain unknown.

METHODS:

We investigated the host T-cell-mediated immune (T-CMI) responses elicited following immunisation with LVS vaccine formulated by the DynPort Vaccine Company (DVC-LVS) or the United States Army Medical Research Institute of Infectious Diseases (USAMRIID-LVS). We compared T-CMI responses prompted by these vaccines and correlated them with take size.

RESULTS:

We found that both LVS vaccines elicited similar T-CMI responses. Interestingly, take size associated with the T cells' ability to proliferate, secrete IFN-γ and mobilise degranulation, suggesting that these responses play an essential role in tularaemia protection.

CONCLUSIONS:

These results renew the appreciation for vaccination through the scarification as a prime route of inoculation to target pathogens driving specific T-CMI responses and provide further evidence that T-CMI plays a role in protection from tularaemia.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Transl Immunology Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Transl Immunology Ano de publicação: 2021 Tipo de documento: Article