Cited by 107Malaria Research and ControlHemoglobinopathies and Related DisordersBlood groups and transfusion

The DOI matches its Crossref record; 108 of the 108 references it cites were found in a registry or an index.

Biochemical and immunological mechanisms by which sickle cell trait protects against malaria

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Abstract

Sickle cell trait (HbAS) is the best-characterized genetic polymorphism known to protect against falciparum malaria. Although the protective effect of HbAS against malaria is well known, the mechanism(s) of protection remain unclear. A number of biochemical and immune-mediated mechanisms have been proposed, and it is likely that multiple complex mechanisms are responsible for the observed protection. Increased evidence for an immune component of protection as well as novel mechanisms, such as enhanced tolerance to disease mediated by HO-1 and reduced parasitic growth due to translocation of host micro-RNA into the parasite, have recently been described. A better understanding of relevant mechanisms will provide valuable insight into the host-parasite relationship, including the role of the host immune system in protection against malaria.

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Crossref · 10.1186/1475-2875-12-317

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Figure 1 Model of mechanisms by which sickle cell trait may protect against malaria.
Figure 1 Model of mechanisms by which sickle cell trait may protect against malaria.CC BY · PubMed Central

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Metadata

Authors
Gong, L., Parikh, S., Rosenthal, P. J., & Greenhouse, B.
Affiliations
  • University of California, San Francisco (US)
  • Yale University (US)
Corresponding author
Greenhouse, Bryan
Venue
Malaria Journal
Published
2013-09-11
Volume
12
Issue
1
Pages
317-317
ISSN
1475-2875 (ISSN-L)
OpenAlex
W2156643348
Cited by
105
References
108
Citations by year
2026: 6 · 2025: 9 · 2024: 4 · 2023: 10 · 2022: 9 · 2021: 8 · 2020: 7 · 2019: 9 · 2018: 12 · 2017: 7 · 2016: 6 · 2015: 12 · 2014: 6
FWCI
1.14
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Malaria Journal (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • eScholarship (California Digital Library) (submittedVersion)
  • eScholarship (California Digital Library) (submittedVersion, cc-by)
Funders
  • Doris Duke Charitable Foundation (2011043)
  • National Institutes of Health
  • U.S. Public Health Service (U19 A1089674)
  • National Institute of Allergy and Infectious Diseases (K23AI076614, U19AI089674)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Malaria Research and Control
  • Health Sciences › Medicine › Genetics (clinical) › Hemoglobinopathies and Related Disorders
  • Health Sciences › Medicine › Hematology › Blood groups and transfusion
Keywords
sickle cell trait, falciparum malaria, malaria prevention, host-parasite interactions, host immune response, heme oxygenase-1, host genetic polymorphisms
MeSH terms
Humans, Sickle Cell Trait, Malaria, Falciparum, Host-Pathogen Interactions

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