CCR5 and CCR5Δ32 in bacterial and parasitic infections: Thinking chemokine receptors outside the HIV box-Reference-Cited by-同舟云学术

CCR5 and CCR5Δ32 in bacterial and parasitic infections: Thinking chemokine receptors outside the HIV box

Published:2020-03-24 Issue:3 Volume:47 Page:261-285
ISSN:1744-3121
Container-title:International Journal of Immunogenetics
language:en
Short-container-title:Int J Immunogenet

Author:

Ellwanger Joel Henrique¹^ORCID,Kaminski Valéria de Lima¹^ORCID,Rodrigues Andressa Gonçalves¹^ORCID,Kulmann‐Leal Bruna¹^ORCID,Chies José Artur Bogo¹^ORCID

Affiliation:

1. Laboratory of Immunobiology and Immunogenetics Department of Genetics Universidade Federal do Rio Grande do Sul – UFRGS Porto Alegre Brazil

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine,Immunology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/iji.12485

Reference258 articles.

1. Circulating HLA-DR+CD4+ effector memory T cells resistant to CCR5 and PD-L1 mediated suppression compromise regulatory T cell function in tuberculosis

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3. Gene Editing of HIV-1 Co-receptors to Prevent and/or Cure Virus Infection

4. CCR5 is a receptor for Staphylococcus aureus leukotoxin ED

5. Staphylococcus aureus and CCR5: unveiling commonalities in host–pathogen interactions and potential treatment strategies

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