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Human Cytomegalovirus Infection in Lung Transplant Recipients Triggers a CXCL‐10 Response
Author(s) -
Weseslindtner L.,
Nachbagauer R.,
Kundi M.,
Jaksch P.,
Kerschner H.,
Simon B.,
HatosAgyi L.,
Scheed A.,
Aberle J.H.,
Klepetko W.,
PuchhammerStöckl E.
Publication year - 2011
Publication title -
american journal of transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.89
H-Index - 188
eISSN - 1600-6143
pISSN - 1600-6135
DOI - 10.1111/j.1600-6143.2010.03404.x
Subject(s) - human cytomegalovirus , bronchoalveolar lavage , medicine , chemokine , immunology , betaherpesvirinae , cytomegalovirus , lung , lung transplantation , viral load , viral replication , virus , inflammation , herpesviridae , viral disease
Human cytomegalovirus (HCMV) causes significant morbidity in lung transplant recipients (LTRs). The clinical effects of HCMV replication are determined partly by a type 1 T‐helper cell (Th1) response. Because the chemokine interferon‐inducible protein of 10 kilodaltons (IP‐10, CXCL‐10) induces a Th1 response, we investigated whether HCMV triggers IP‐10 in LTRs. The IP‐10 concentration and HCMV DNA load were determined in 107 plasma and 46 bronchoalveolar lavage fluid (BALF) samples from 36 LTRs. Initial HCMV detection posttransplantation was significantly associated with increased plasma IP‐10, regardless of whether the patients showed HCMV DNAemia (p = 0.001) or HCMV replication only in the allograft (p < 0.0001). In subsequent episodes of HCMV detection, plasma IP‐10 increased regardless of whether HCMV was detected in blood (p = 0.0078) or only in BALF (p < 0.0001) and decreased after successful antiviral therapy (p = 0.0005). Furthermore, levels of HCMV DNA and IP‐10 correlated statistically (p = 0.0033). Increased IP‐10 levels in HCMV‐positive BALF samples were significantly associated with severe airflow obstruction, as indicated by a decrease in forced expiratory volume in one second (FEV1). Our data indicate that HCMV replication in LTRs evokes a plasma IP‐10 response and that, when an IP‐10 response is observed in BALF, it is associated with inflammatory airway obstruction in the allograft.