DESCRIPTION

The Cd40l^{–/–} mouse is a well-established model of X-linked hyper-immunoglobulin M (IgM) syndrome, an immunodeficiency disorder of human beings characterized by the lack of expression of the CD40 ligand (CD40L) on activated T-cells, predisposing to infections with opportunistic pathogens like Pneumocystis jirovecii. The aim of our study was to describe the pulmonary lesions in Cd40l^{–/–} mice experimentally infected with Pneumocystis murina, in comparison with naturally infected severe combined immunodeficient (SCID) mice.

Formalin-fixed paraffin-embedded lungs from 26 Cd40l^{–/–}, 11 SCID, and 5 uninfected Cd40l^{–/–} mice were examined by histology and immunohistochemistry for the presence of the pathogen and for leukocyte populations (CD3, CD4, CD45R/B220, CD8a, Iba-1, Ly-6G, CD206, MHC II, and NKp46/NCR1).

Infection was confirmed by immunohistochemistry in 18/26 (69%) Cd40l^{–/–} mice and in 11/11 (100%) SCID mice. Fourteen out of 26 (54%) Cd40l^{–/–} mice had interstitial pneumonia. Twenty-three out of 26 (88%) Cd40l^{–/–} mice had peribronchiolar/perivascular lymphoplasmacytic infiltrates, rich in B-cells and Mott cells. Acidophilic macrophage pneumonia was additionally found in 20/26 (77%) Cd40l^{–/–} mice.

Only 4/11 (36%) SCID mice had interstitial pneumonia, but no peribronchiolar/perivascular infiltrates or acidophilic macrophage pneumonia were observed in this strain. This study represents the first description of pulmonary histopathological lesions in Cd40l^{–/–} mice infected with P. murina. We speculate that the singular characteristics of the inflammatory infiltrates observed in Cd40l^{–/–} mice could be explained by the specific immune phenotype of the model.

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