Elderly-onset hereditary pulmonary alveolar proteinosis and its cytokine profile-Reference-Cited by-同舟云学术

Elderly-onset hereditary pulmonary alveolar proteinosis and its cytokine profile

Published:2017-02-17 Issue:1 Volume:17 Page:
ISSN:1471-2466
Container-title:BMC Pulmonary Medicine
language:en
Short-container-title:BMC Pulm Med

Author:

Ito Masayuki,Nakagome Kazuyuki,Ohta Hiromitsu,Akasaka Keiichi,Uchida Yoshitaka,Hashimoto Atsushi,Shiono Ayako,Takada Toshinori,Nagata Makoto,Tohyama Jun,Hagiwara Koichi,Kanazawa Minoru,Nakata Koh,Tazawa Ryushi^ORCID

Funder

Ministry of Health, Labor and Welfare of Japan

Grant-in-Aid for Scientific Research

Japan Agency for Medical Research and Development

Publisher

Springer Science and Business Media LLC

Subject

Pulmonary and Respiratory Medicine

Link

http://link.springer.com/content/pdf/10.1186/s12890-017-0382-x.pdf

Reference20 articles.

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2. Seymour JF, Presneill JJ. Pulmonary alveolar proteinosis: progress in the first 44 years. Am J Respir Crit Care Med. 2002;166:215–35.

3. Trapnell BC, Whitsett JA, Nakata K. Pulmonary alveolar proteinosis. N Engl J Med. 2003;349:2527–39.

4. Kitamura T, Tanaka N, Watanabe J. Uchida, Kanegasaki S, Yamada Y, Nakata K. Idiopathic pulmonary alveolar proteinosis as an autoimmune disease with neutralizing antibody against granulocyte/macrophage colony-stimulating factor. J Exp Med. 1999;190:875–80.

5. Uchida K, Nakata K, Trapnell BC, Terakawa T, Hamano E, Mikami A, Matsushita I, Seymour JF, Oh-Eda M, Ishige I, Eishi Y, Kitamura T, Yamada Y, Hanaoka K, Keicho N. High-affinity autoantibodies specifically eliminate granulocyte-macrophage colony-stimulating factor activity in the lungs of patients with idiopathic pulmonary alveolar proteinosis. Blood. 2004;103:1089–98.

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