Morphological and cytochemical characterization of cells infiltrating mouse lungs after influenza infection
- PMID: 711312
- PMCID: PMC421968
- DOI: 10.1128/iai.21.1.140-146.1978
Morphological and cytochemical characterization of cells infiltrating mouse lungs after influenza infection
Abstract
To initiate evaluation of the cell-mediated immunological response to influenza virus in a major site of disease, lung cells were obtained by transpleural lavage from lungs of uninfected mice and from those infected 3 or 6 days previously with 5 50% mouse infectious doses (MID(50)) of avirulent (P3) or virulent (P9) influenza A Hong Kong (H3N2) virus. The number of cells recovered by lavage was dependent on the dose, time after inoculation, and the type of virus used for inoculation. Although lavage pools were shown to contain peripheral blood leukocytes, this contamination was shown to be consistently less than 5% of the total leukocytes harvested. Among the ca. 0.75 x 10(6) lavage cells obtained from each uninfected mouse, about 90% were macrophages or lymphocytes in approximately equal proportion. T, B, and null (lyphocytes lacking theta or surface immunoglobulin markers) lymphocytes averaged 23, 9, and 7% of cells in these suspensions, respectively. After infection with either P3 or P9 virus, increased numbers of activated macrophages and lymphoblasts were observed. The major change during P3 infection was an increase in absolute numbers of null lymphocytes. In contrast, during P9 infection, T and B lymphocytes and macrophages progressively increased in absolute numbers while null cells decreased. These data suggest that cell-mediated immunological responses to influenza virus occur in the lung during infection, but that the responses to virulent and avirulent variants may differ both qualitatively and quantitatively.
Similar articles
-
Cellular changes in lungs of mice infected with influenza virus: characterization of the cytotoxic responses.Infect Immun. 1978 Nov;22(2):423-9. doi: 10.1128/iai.22.2.423-429.1978. Infect Immun. 1978. PMID: 310424 Free PMC article.
-
Interferon production by leukocytes infiltrating the lungs of mice during primary influenza virus infection.Infect Immun. 1982 Dec;38(3):1249-55. doi: 10.1128/iai.38.3.1249-1255.1982. Infect Immun. 1982. PMID: 6295944 Free PMC article.
-
Alveolitis induced by influenza virus.Am Rev Respir Dis. 1983 Oct;128(4):730-9. doi: 10.1164/arrd.1983.128.4.730. Am Rev Respir Dis. 1983. PMID: 6625351
-
Effects of low- and high-passage influenza virus infection in normal and nude mice.Infect Immun. 1977 Jan;15(1):221-9. doi: 10.1128/iai.15.1.221-229.1977. Infect Immun. 1977. PMID: 832899 Free PMC article.
-
Therapeutic effect of erythromycin on influenza virus-induced lung injury in mice.Am J Respir Crit Care Med. 1998 Mar;157(3 Pt 1):853-7. doi: 10.1164/ajrccm.157.3.9703098. Am J Respir Crit Care Med. 1998. PMID: 9517602
Cited by
-
Human Alveolar Macrophages May Not Be Susceptible to Direct Infection by a Human Influenza Virus.J Infect Dis. 2016 Dec 1;214(11):1658-1665. doi: 10.1093/infdis/jiw413. Epub 2016 Sep 6. J Infect Dis. 2016. PMID: 27601618 Free PMC article.
-
Influenza A virus replication is inhibited by tumor necrosis factor-alpha in vitro.Arch Virol. 1994;136(3-4):439-46. doi: 10.1007/BF01321073. Arch Virol. 1994. PMID: 8031247
-
Alterations of pulmonary defense mechanisms by protein depletion diet.Infect Immun. 1981 Nov;34(2):610-22. doi: 10.1128/iai.34.2.610-622.1981. Infect Immun. 1981. PMID: 7309243 Free PMC article.
-
Alterations in lung macrophage antimicrobial activity associated with viral pneumonia.Infect Immun. 1979 Nov;26(2):492-7. doi: 10.1128/iai.26.2.492-497.1979. Infect Immun. 1979. PMID: 232689 Free PMC article.
-
Enhancement of bronchoalveolar cell recovery and stimulation of alveolar macrophage chemiluminescence and resistance to influenza virus after treatment with RU 41821 aerosol.Antimicrob Agents Chemother. 1987 Jun;31(6):920-4. doi: 10.1128/AAC.31.6.920. Antimicrob Agents Chemother. 1987. PMID: 3619424 Free PMC article.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources