Constitutive expression of types 1 and 2 cytokines by alveolar macrophages from feline immunodeficiency virus-infected cats

• Published in: Veterinary immunology and immunopathology 2001-05, Vol.79 (1), p.83-100
• Main Authors: Ritchey, Jerry W, Levy, Julie K, Bliss, Susan K, Tompkins, Wayne A.F, Tompkins, Mary B
• Format: Article
• Language: English
• Subjects: Animals; Bronchoalveolar lavage; Bronchoalveolar Lavage - veterinary; Cat Diseases - metabolism; Cats; Feline Acquired Immunodeficiency Syndrome - metabolism; feline immunodeficiency virus; FIV; gag gene; Gene Products, gag - biosynthesis; Immunodeficiency Virus, Feline; Interleukin-10 - biosynthesis; Interleukin-12 - biosynthesis; Interleukin-6 - biosynthesis; Interleukins; Macrophages; Macrophages, Alveolar - metabolism; Male; Reverse Transcriptase Polymerase Chain Reaction - veterinary; RNA, Messenger - metabolism; tumor necrosis factor-^a; Tumor Necrosis Factor-alpha - biosynthesis; Viral Envelope Proteins - biosynthesis
• ISSN: 0165-2427; 1873-2534
• DOI: 10.1016/S0165-2427(01)00250-1

Evidence suggests that feline immunodeficiency virus (FIV), causes pulmonary immunodeficiency. The overall objective of this study was to explore FIV-induced alterations in cell counts and cytokine gene expression in the pulmonary compartment during the acute stage infection. Bronchoalveolar lavage (BAL) cells were collected from FIV-infected and control cats at 0, 4, 10, and 16 weeks post-FIV infection for phenotype and cytokine analysis. The major change in BAL cellular populations following FIV-infection was the development of a neutrophilia. Total BAL cell counts and relative numbers of alveolar macrophages (AM), eosinophils, and lymphocytes remained similar in both groups. The RT-qcPCR analyses of AM purified from BAL showed constitutive expression of TNFα, IL6 and IL10 mRNAs that peaked during the acute stage of infection then declined. The TNFα and IL6 bioactive protein secretion showed a similar response. In contrast, IFNγ expression increased progressively with time after infection and paralleled a progressive increase in FIV-gag mRNA in AM. The IL12 p40 expression also differed from the other cytokines in that there was a progressive decrease in the number of cats with AM IL12 expression following FIV infection. Infection of AM in vitro with FIV also caused an increase in TNFα and IL6 mRNA and bioactive protein suggesting that the increased cytokine response by AM following infection of cats with FIV is an intrinsic characteristic of FIV-infected AM. In summary, pulmonary immune changes seen in FIV-infected cats are similar to those seen in HIV-infected human patients.