Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1974 Mar;9(3):534–539. doi: 10.1128/iai.9.3.534-539.1974

Effects of Carbon Dust Inhalation on the Cell-Mediated Immune Response in Mice 1

S D Miller a, A Zarkower a
PMCID: PMC414840  PMID: 4206026

Abstract

The effects of carbon dust inhalation on the bone marrow-derived (B) and thymus-derived (T) lymphocyte populations of spleen and mediastinal lymph node (MLN) cultures were examined. The concanavalin A (Con A)-responsive cell population (T cells) in the spleen was found to be depressed after 7 days of pre-exposure to carbon dust. However, this effect was transient, and after 14, 21, and 28 days of pre-exposure to carbon dust, the Con A-responsive cells exhibited a 30 to 40% enhancement over control group responses. Conversely, Con A-responsive cells in the pooled MLN cultures exhibited depression, ranging from 22 to 33% below control group values, after 7, 14, and 28 days of pre-exposure to carbon dust. The lipopolysaccharide (LPS)-responsive cell population (B cells) in the spleens of carbon-exposed mice was found not to differ significantly from control group values after all times of pre-exposure. LPS-responsive cells in the MLN cultures exhibited enhancement, ranging from 49 to 74% above control values, after 14, 21, and 28 days of pre-exposure to carbon dust. The ability of carbon spleen cell cultures from carbon-exposed mice to undergo antigen induced blast transformation after sensitization with Mycobacterium tuberculosis H37Ra was also determined. Mice exposed to carbon dust inhalation 2 weeks before and 3 weeks after aerosol or subcutaneous immunization exhibited significantly enhanced ratios of transformation upon culture of their spleen lymphocytes with purified protein derivative of tuberculin.

Full text

PDF
534

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Adler W. H., Takiguchi T., Marsh B., Smith R. T. Cellular recognition by mouse lymphocytes in vitro. I. Definition of a new technique and results of stimulation by phytohemagglutinin and specific antigens. J Exp Med. 1970 Jun 1;131(6):1049–1078. doi: 10.1084/jem.131.6.1049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Andersson J., Möller G., Sjöberg O. Selective induction of DNA synthesis in T and B lymphocytes. Cell Immunol. 1972 Aug;4(4):381–393. doi: 10.1016/0008-8749(72)90040-8. [DOI] [PubMed] [Google Scholar]
  3. BOREN H. G. CARBON AS A CARRIER MECHANISM FOR IRRITANT GASES. Arch Environ Health. 1964 Jan;8:119–124. doi: 10.1080/00039896.1964.10663639. [DOI] [PubMed] [Google Scholar]
  4. Bloom B. R. In vitro approaches to the mechanism of cell-mediated immune reactions. Adv Immunol. 1971;13:101–208. doi: 10.1016/s0065-2776(08)60184-4. [DOI] [PubMed] [Google Scholar]
  5. Fisher S. Stimulation of splenic antigen uptake and of antibody response in mice by India ink or other "blockading" agents. Immunology. 1966 Aug;11(2):127–136. [PMC free article] [PubMed] [Google Scholar]
  6. Green G. M. The J. Burns Amberson Lecture--in defense of the lung. Am Rev Respir Dis. 1970 Nov;102(5):691–703. doi: 10.1164/arrd.1970.102.5.691. [DOI] [PubMed] [Google Scholar]
  7. Hinners R. G., Burkart J. K., Punte C. L. Animal inhalation exposure chambers. Arch Environ Health. 1968 Feb;16(2):194–206. doi: 10.1080/00039896.1968.10665043. [DOI] [PubMed] [Google Scholar]
  8. MIDDLEBROOK G. An apparatus for airborne infection of mice. Proc Soc Exp Biol Med. 1952 May;80(1):105–110. doi: 10.3181/00379727-80-19538. [DOI] [PubMed] [Google Scholar]
  9. Möller G., Michael G. Frequency of antigen-sensitive cells to thymus-independent antigens. Cell Immunol. 1971 Aug;2(4):309–316. doi: 10.1016/0008-8749(71)90065-7. [DOI] [PubMed] [Google Scholar]
  10. NAU C. A., NEAL J., STEMBRIDGE V. A., COOLEY R. N. Physiological effects of carbon black. IV. Inhalation. Arch Environ Health. 1962 Apr;4:415–431. doi: 10.1080/00039896.1962.10663179. [DOI] [PubMed] [Google Scholar]
  11. Peavy D. L., Adler W. H., Smith R. T. The mitogenic effects of endotoxin and staphylococcal enterotoxin B on mouse spleen cells and human peripheral lymphocytes. J Immunol. 1970 Dec;105(6):1453–1458. [PubMed] [Google Scholar]
  12. Rylander R. Alterations of lung defense mechanisms against airborne bacteria. Arch Environ Health. 1969 Apr;18(4):551–555. doi: 10.1080/00039896.1969.10665452. [DOI] [PubMed] [Google Scholar]
  13. Rylander R. Pulmonary defence mechanisms to airborne bacteria. Acta Physiol Scand Suppl. 1968;306:1–89. [PubMed] [Google Scholar]
  14. Rylander R. Studies of lung defense to infections in inhalation toxicology. Arch Intern Med. 1970 Sep;126(3):496–499. [PubMed] [Google Scholar]
  15. Sabet T. Y., Friedman H. Effects of RES "blockade" on antibody formation. II. Cytokinetics of the secondary haemolysin response and suppressed immunological "memory" in mice treated with carbon particles. Immunology. 1969 Oct;17(4):535–550. [PMC free article] [PubMed] [Google Scholar]
  16. Sabet T., Newlin C., Friedman H. Effects of RES "blockade" on antibody-formation. I. Suppressed cellular and humoral haemolysin responses in mice injected with carbon particles. Immunology. 1969 Apr;16(4):433–446. [PMC free article] [PubMed] [Google Scholar]
  17. Zarkower A. Alterations in antibody response induced by chronic inhalation of SO 2 and carbon. Arch Environ Health. 1972 Jul;25(1):45–50. doi: 10.1080/00039896.1972.10666134. [DOI] [PubMed] [Google Scholar]
  18. Zarkower A., Morges W. Alteration in antibody response induced by carbon inhalation: a model system. Infect Immun. 1972 Jun;5(6):915–920. doi: 10.1128/iai.5.6.915-920.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES