Cited by 1,839Mast cells and histamineAsthma and respiratory diseasesAllergic Rhinitis and Sensitization

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The development of allergic inflammation

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Galli, Stephen J., Tsai, Mindy, Piliponsky, Adrian M.·2008·Nature

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Abstract

Allergic disorders, such as anaphylaxis, hay fever, eczema and asthma, now afflict roughly 25% of people in the developed world. In allergic subjects, persistent or repetitive exposure to allergens, which typically are intrinsically innocuous substances common in the environment, results in chronic allergic inflammation. This in turn produces long-term changes in the structure of the affected organs and substantial abnormalities in their function. It is therefore important to understand the characteristics and consequences of acute and chronic allergic inflammation, and in particular to explore how mast cells can contribute to several features of this maladaptive pattern of immunological reactivity.

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Vignali, D. A. A., Collison, L. W., & Workman, C. J. (2008) · Nature Reviews Immunology · doi:10.1038/nri2343 · Cited by 3,463
Anesthesiology
Wiklund, R. A., & Rosenbaum, S. H. (1997) · New England Journal of Medicine · doi:10.1056/nejm199710163371606 · Cited by 2,153
REGULATION OF IMMUNE RESPONSES BY TGF-β
Letterio, J. J., & Roberts, A. B. (1998) · Annual Review of Immunology · doi:10.1146/annurev.immunol.16.1.137 · Cited by 1,894
Anti-Inflammatory Cytokines
Opal, S. M., & DePalo, V. A. (2000) · Chest · doi:10.1378/chest.117.4.1162 · Cited by 1,752
The asthma epidemic
Eder, W., Ege, M. J., & von Mutius, E. (2006) · New England Journal of Medicine · doi:10.1056/nejmra054308 · Cited by 1,621
Allergy, Parasites, and the Hygiene Hypothesis
Yazdanbakhsh, M., Kremsner, P. G., & van Ree, R. (2002) · Science · doi:10.1126/science.296.5567.490 · Cited by 1,527
Immunology of asthma and chronic obstructive pulmonary disease
Barnes, P. J. (2008) · Nature reviews. Immunology · doi:10.1038/nri2254 · Cited by 1,444
New insights into atopic dermatitis
Leung, D. Y. M., Boguniewicz, M., Howell, M. D., Nomura, I., & Hamid, Q. A. (2004) · Journal of Clinical Investigation · doi:10.1172/jci21060 · Cited by 1,435
Allergy and Allergic Diseases
Kay, A. B. (2001) · New England Journal of Medicine · doi:10.1056/nejm200101043440106 · Cited by 1,368
MAST CELLS AS “TUNABLE” EFFECTOR AND IMMUNOREGULATORY CELLS: Recent Advances
Galli, S. J., Kalesnikoff, J., Grimbaldeston, M. A., Piliponsky, A. M., Williams, C. M. M., & Tsai, M. M. (2005) · Annual Review of Immunology · doi:10.1146/annurev.immunol.21.120601.141025 · Cited by 1,259
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von Pirquet, C. Allergie. Münch. Med. Wochenschr. 53, 1457–1458 (1906).

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Authors: Galli, S. J., Tsai, M., & Piliponsky, A. M.
Affiliations: Stanford Medicine (US)
ORCID: Galli, Stephen J.
Tsai, Mindy
Piliponsky, Adrian M.
Venue: Nature
Publisher: Springer Science and Business Media LLC
Published: 2008-07-01
Volume: 454
Issue: 7203
Pages: 445-454
ISSN: 0028-0836 (ISSN-L)
1476-4687
DOI: 10.1038/nature07204
PMC: PMC3573758
OpenAlex: W2007589345
Cited by: 1,839
References: 102
Citations by year: 2026: 75 · 2025: 80 · 2024: 100 · 2023: 127 · 2022: 117 · 2021: 113 · 2020: 133 · 2019: 125 · 2018: 97 · 2017: 101 · 2016: 102 · 2015: 94 · 2014: 124 · 2013: 106 · 2012: 95
FWCI: 6.11
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.springer.com/tdm (tdm)
www.springer.com/tdm (vor)
Locations: Nature (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
RePEc: Research Papers in Economics (submittedVersion)
Funders: National Institutes of Health
National Cancer Institute (R01CA072074)
National Institute of Allergy and Infectious Diseases (R01AI023990, R01AI070813)
Topics: Life Sciences › Immunology and Microbiology › Immunology › Mast cells and histamine
Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Asthma and respiratory diseases
Health Sciences › Medicine › Immunology and Allergy › Allergic Rhinitis and Sensitization
Keywords: allergic inflammation, mast cells, anaphylaxis, allergic rhinitis, atopic dermatitis, asthma, allergen exposure, chronic inflammation, hypersensitivity
MeSH terms: Allergens, Animals, Chronic Disease, Epithelium, Humans, Hypersensitivity, Immunoglobulin E, Inflammation

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