Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2011 Aug;165(2):278-84.
doi: 10.1111/j.1365-2249.2011.04422.x. Epub 2011 May 23.

Lack of evidence of CD40 ligand involvement in transfusion-related acute lung injury

Affiliations

Lack of evidence of CD40 ligand involvement in transfusion-related acute lung injury

P R Tuinman et al. Clin Exp Immunol. 2011 Aug.

Abstract

Activated platelets have been implicated in playing a major role in transfusion-related acute lung injury (TRALI), as platelets can trigger neutrophils, resulting in vascular damage. We hypothesized that binding of platelet CD40 ligand (CD40L) to endothelial CD40 is essential in the onset of TRALI. Mice were challenged with monoclonal major histocompatibility complex (MHC)-1 antibody which induced TRALI, evidenced by pulmonary oedema, accompanied by significantly elevated bronchoalveolar fluid (BALF) levels of total protein and elevated plasma levels of keratinocyte-derived chemokine (KC) and macrophage inflammatory protein-2 (MIP-2) compared to infusion of isotype antibody (all Ps < 0·05). Treatment with ciglitazone, which inhibits platelet CD40L expression, had no effect on pulmonary and systemic inflammation compared to controls. In addition, treatment with anti-CD40L antibody, which antagonizes all CD40-CD40L interactions, also did not abrogate the TRALI reaction. Furthermore, levels of soluble CD40L were measured in a cohort of cardiac surgery patients, who were followed prospectively for the onset of TRALI after transfusion. Plasma levels of sCD40L at baseline and at time of developing TRALI did not differ between TRALI patients and controls (transfused cardiac surgery patients not developing acute lung injury) (275 ± 192 versus 258 ± 346 and 93 ± 82 versus 93 ± 123 pg/ml, respectively, not significant). In conclusion, these results do not support the idea that the CD40-CD40L interaction is involved in mediating TRALI.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Pulmonary oedema and protein leakage after induction of transfusion-related acute lung injury and treatment with anti-CD40 ligand antibody or ciglitazone and controls. *P < 0·05; **P < 0·01.
Fig. 2
Fig. 2
Levels of chemoattractants in broncoalveolar lavage fluid (BALF; upper panels) and plasma (lower panels) after induction of transfusion-related acute lung injury and treatment with anti-CD40 ligand antibody or ciglitazone and controls. KC: keratinocyte-derived chemokine; MIP-2: macrophage-inflammatory protein-2.
Fig. 3
Fig. 3
Plasma levels of sCD40 ligand and platelet count before and after cardiac surgery in transfusion-related acute lung injury (TRALI) patients and transfused controls.

Similar articles

Cited by

References

    1. Goldman M, Webert KE, Arnold DM, Freedman J, Hannon J, Blajchman MA. Proceedings of a consensus conference: towards an understanding of TRALI. Transfus Med Rev. 2005;19:2–31. - PubMed
    1. Silliman CC. The two-event model of transfusion-related acute lung injury. Crit Care Med. 2006;34:S124–S131. - PubMed
    1. Silliman CC, Boshkov LK, Mehdizadehkashi Z, et al. Transfusion-related acute lung injury: epidemiology and a prospective analysis of etiologic factors. Blood. 2003;101:454–62. - PubMed
    1. Bux J. Antibody-mediated (immune) transfusion-related acute lung injury. Vox Sang. 2011;100:122–8. - PubMed
    1. Silliman CC, Paterson AJ, Dickey WO, et al. The association of biologically active lipids with the development of transfusion-related acute lung injury: a retrospective study. Transfusion. 1997;37:719–26. - PubMed

MeSH terms