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Novel adaptive and innate immunity targets in hypertension

*Corresponding author for this work
  • Medical College of Wisconsin
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Hypertension is a worldwide epidemic and global health concern as it is a major risk factor for the development of cardiovascular diseases. A relationship between the immune system and its contributing role to the pathogenesis of hypertension has been long established, but substantial advancements within the last few years have dissected specific causal molecular mechanisms. This review will briefly examine these recent studies exploring the involvement of either innate or adaptive immunity pathways. Such pathways to be discussed include innate immunity factors such as antigen presenting cells and pattern recognition receptors, adaptive immune elements including T and B lymphocytes, and more specifically, the emerging role of T regulatory cells, as well as the potential of cytokines and chemokines to serve as signaling messengers connecting innate and adaptive immunity. Together, we summarize these studies to provide new perspective for what will hopefully lead to more targeted approaches to manipulate the immune system as hypertensive therapy.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 109-115 (7 pages)

Journal (Volume, Issue Number)

Pharmacological Research (Volume 120)

Publication milestones

  • Published - 06/01/2017

Publication status

Published - 06/01/2017

ISSN

1043-6618

Publication IDs

  • Scopus: 85016433007
  • PubMed: 28336371

Publication metrics

Metrics

SciVal
FWCI
0.30
SciVal
Author count
4
SciVal
citations
8
SciVal
Paper percentile
71
Fractional count
2
Fractional count
0.50
Fractional count
2
Fractional count
0.50
Fractional count
2
Fractional count
1
Scopus
citations

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Captures
39
Citation count
12

Funding Details

FunderFunding number
NIDDK
R01DK096859