Expression of Lymphocytes and Lymphocyte Subsets in Patients with Severe Acute Respiratory Syndrome
Identifieur interne : 000839 ( Pmc/Curation ); précédent : 000838; suivant : 000840Expression of Lymphocytes and Lymphocyte Subsets in Patients with Severe Acute Respiratory Syndrome
Auteurs : Wei Cui ; Ying Fan ; Wei Wu ; Feng Zhang ; Jun-Ying Wang ; An-Ping NiSource :
- Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America [ 1058-4838 ] ; 2003.
Abstract
In a cohort of 38 patients with severe acute respiratory syndrome (SARS), we observed leukopenia in 47% of patients, lymphopenia in 84%, and T lymphopenia in 95%. CD4+ T lymphocyte levels were reduced in 100% of patients, CD8+ T lymphocyte levels were reduced in 87%, B lymphocyte levels were reduced in 76%, and natural killer cell levels were reduced in 55%. Our data suggested that these patients' immune systems were impaired during the course of SARS. The absolute counts of lymphocyte subsets demonstrated a clinical significance for patients with SARS.
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DOI: 10.1086/378587
PubMed: 12955652
PubMed Central: 7110124
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<p>In a cohort of 38 patients with severe acute respiratory syndrome (SARS), we observed leukopenia in 47% of patients, lymphopenia in 84%, and T lymphopenia in 95%. CD4<sup>+</sup>
T lymphocyte levels were reduced in 100% of patients, CD8<sup>+</sup>
T lymphocyte levels were reduced in 87%, B lymphocyte levels were reduced in 76%, and natural killer cell levels were reduced in 55%. Our data suggested that these patients' immune systems were impaired during the course of SARS. The absolute counts of lymphocyte subsets demonstrated a clinical significance for patients with SARS.</p>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">Clin Infect Dis</journal-id>
<journal-id journal-id-type="iso-abbrev">Clin. Infect. Dis</journal-id>
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<article-categories><subj-group subj-group-type="heading"><subject>Brief Reports</subject>
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<title-group><article-title>Expression of Lymphocytes and Lymphocyte Subsets in Patients with Severe Acute Respiratory Syndrome</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Cui</surname>
<given-names>Wei</given-names>
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<xref ref-type="corresp" rid="cor1"></xref>
<xref ref-type="aff" rid="d352119e128"></xref>
<pmc-comment>mawx@csc.pumch.ac.cn </pmc-comment>
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<contrib contrib-type="author"><name><surname>Fan</surname>
<given-names>Ying</given-names>
</name>
<xref ref-type="aff" rid="d352119e128"></xref>
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<contrib contrib-type="author"><name><surname>Wu</surname>
<given-names>Wei</given-names>
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<contrib contrib-type="author"><name><surname>Zhang</surname>
<given-names>Feng</given-names>
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<contrib contrib-type="author"><name><surname>Wang</surname>
<given-names>Jun-ying</given-names>
</name>
<xref ref-type="aff" rid="d352119e128"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Ni</surname>
<given-names>An-ping</given-names>
</name>
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</contrib>
</contrib-group>
<aff id="d352119e128"><institution>Department of Clinical Laboratory, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences</institution>
,<addr-line>Beijing, People's Republic of China</addr-line>
</aff>
<author-notes><corresp id="cor1">Reprints or correspondence: Dr. Wei Cui, Dept. of Clinical Laboratory, Peking Union Medical College Hospital, 1 Shuaifuyuan Wangfujing, Beijing, 100730, People's Republic of China (<email>mawx@csc.pumch.ac.cn</email>
).</corresp>
</author-notes>
<pub-date pub-type="ppub"><day>15</day>
<month>9</month>
<year>2003</year>
</pub-date>
<pub-date pub-type="epub" iso-8601-date="2003-09-15"><day>15</day>
<month>9</month>
<year>2003</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>15</day>
<month>9</month>
<year>2003</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on the . </pmc-comment>
<volume>37</volume>
<issue>6</issue>
<fpage>857</fpage>
<lpage>859</lpage>
<history><date date-type="received"><day>1</day>
<month>6</month>
<year>2003</year>
</date>
<date date-type="accepted"><day>16</day>
<month>7</month>
<year>2003</year>
</date>
</history>
<permissions><copyright-statement>© 2003 by the Infectious Diseases Society of America</copyright-statement>
<copyright-year>2003</copyright-year>
<license><license-p>This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.</license-p>
</license>
</permissions>
<self-uri xlink:href="37-6-857.pdf"></self-uri>
<abstract><title>Abstract</title>
<p>In a cohort of 38 patients with severe acute respiratory syndrome (SARS), we observed leukopenia in 47% of patients, lymphopenia in 84%, and T lymphopenia in 95%. CD4<sup>+</sup>
T lymphocyte levels were reduced in 100% of patients, CD8<sup>+</sup>
T lymphocyte levels were reduced in 87%, B lymphocyte levels were reduced in 76%, and natural killer cell levels were reduced in 55%. Our data suggested that these patients' immune systems were impaired during the course of SARS. The absolute counts of lymphocyte subsets demonstrated a clinical significance for patients with SARS.</p>
</abstract>
</article-meta>
</front>
</pmc>
</record>
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