Primary role for CD4(+) T lymphocytes in recovery from oropharyngeal candidiasis. 2002

C S Farah, and S Elahi, and K Drysdale, and G Pang, and T Gotjamanos, and G J Seymour, and R L Clancy, and R B Ashman
Oral Biology and Pathology, School of Dentistry, University of Queensland, Brisbane, Queensland, Australia. c.farah@uq.edu.au

Oropharyngeal candidiasis is associated with defects in cell-mediated immunity and is commonly seen in human immunodeficiency virus positive individuals and AIDS patients. A model for oral candidiasis in T-cell-deficient BALB/c and CBA/CaH nu/nu mice was established. After inoculation with 10(8) Candida albicans yeasts, these mice displayed increased levels of oral colonization compared to euthymic control mice and developed a chronic oropharyngeal infection. Histopathological examination of nu/nu oral tissues revealed extensive hyphae penetrating the epithelium, with polymorphonuclear leukocyte microabscess formation. Adoptive transfer of either naive or immune lymphocytes into immunodeficient mice resulted in the recovery of these animals from the oral infection. Reconstitution of immunodeficient mice with naive CD4(+) but not CD8(+) T cells significantly decreased oral colonization compared to controls. Interleukin-12 and gamma interferon were detected in the draining lymph nodes of immunodeficient mice following reconstitution with naive lymphocytes. This study demonstrates the direct requirement for T lymphocytes in recovery from oral candidiasis and suggests that this is associated with the production of cytokines by CD4(+) T helper cells.

UI MeSH Term Description Entries
D008198 Lymph Nodes They are oval or bean shaped bodies (1 - 30 mm in diameter) located along the lymphatic system. Lymph Node,Node, Lymph,Nodes, Lymph
D008214 Lymphocytes White blood cells formed in the body's lymphoid tissue. The nucleus is round or ovoid with coarse, irregularly clumped chromatin while the cytoplasm is typically pale blue with azurophilic (if any) granules. Most lymphocytes can be classified as either T or B (with subpopulations of each), or NATURAL KILLER CELLS. Lymphoid Cells,Cell, Lymphoid,Cells, Lymphoid,Lymphocyte,Lymphoid Cell
D008807 Mice, Inbred BALB C An inbred strain of mouse that is widely used in IMMUNOLOGY studies and cancer research. BALB C Mice, Inbred,BALB C Mouse, Inbred,Inbred BALB C Mice,Inbred BALB C Mouse,Mice, BALB C,Mouse, BALB C,Mouse, Inbred BALB C,BALB C Mice,BALB C Mouse
D008808 Mice, Inbred CBA An inbred strain of mouse that is widely used in BIOMEDICAL RESEARCH. Mice, CBA,Mouse, CBA,Mouse, Inbred CBA,CBA Mice,CBA Mice, Inbred,CBA Mouse,CBA Mouse, Inbred,Inbred CBA Mice,Inbred CBA Mouse
D008819 Mice, Nude Mutant mice homozygous for the recessive gene "nude" which fail to develop a thymus. They are useful in tumor studies and studies on immune responses. Athymic Mice,Mice, Athymic,Nude Mice,Mouse, Athymic,Mouse, Nude,Athymic Mouse,Nude Mouse
D010612 Pharyngitis Inflammation of the throat (PHARYNX). Sore Throat,Pharyngitides,Sore Throats,Throat, Sore
D002176 Candida albicans A unicellular budding fungus which is the principal pathogenic species causing CANDIDIASIS (moniliasis). Candida albicans var. stellatoidea,Candida stellatoidea,Dematium albicans,Monilia albicans,Myceloblastanon albicans,Mycotorula albicans,Parasaccharomyces albicans,Procandida albicans,Procandida stellatoidea,Saccharomyces albicans,Syringospora albicans
D002177 Candidiasis Infection with a fungus of the genus CANDIDA. It is usually a superficial infection of the moist areas of the body and is generally caused by CANDIDA ALBICANS. (Dorland, 27th ed) Candida Infection,Moniliasis,Candida Infections,Candidiases,Infection, Candida,Moniliases
D004195 Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. Animal Disease Model,Animal Disease Models,Disease Model, Animal
D004797 Enzyme-Linked Immunosorbent Assay An immunoassay utilizing an antibody labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed. ELISA,Assay, Enzyme-Linked Immunosorbent,Assays, Enzyme-Linked Immunosorbent,Enzyme Linked Immunosorbent Assay,Enzyme-Linked Immunosorbent Assays,Immunosorbent Assay, Enzyme-Linked,Immunosorbent Assays, Enzyme-Linked

Related Publications

C S Farah, and S Elahi, and K Drysdale, and G Pang, and T Gotjamanos, and G J Seymour, and R L Clancy, and R B Ashman
July 1991, Infection and immunity,
C S Farah, and S Elahi, and K Drysdale, and G Pang, and T Gotjamanos, and G J Seymour, and R L Clancy, and R B Ashman
February 2009, The Journal of experimental medicine,
C S Farah, and S Elahi, and K Drysdale, and G Pang, and T Gotjamanos, and G J Seymour, and R L Clancy, and R B Ashman
August 1977, Infection and immunity,
C S Farah, and S Elahi, and K Drysdale, and G Pang, and T Gotjamanos, and G J Seymour, and R L Clancy, and R B Ashman
January 2019, Frontiers in immunology,
C S Farah, and S Elahi, and K Drysdale, and G Pang, and T Gotjamanos, and G J Seymour, and R L Clancy, and R B Ashman
January 2003, Advances in cancer research,
C S Farah, and S Elahi, and K Drysdale, and G Pang, and T Gotjamanos, and G J Seymour, and R L Clancy, and R B Ashman
January 2015, Frontiers in physiology,
C S Farah, and S Elahi, and K Drysdale, and G Pang, and T Gotjamanos, and G J Seymour, and R L Clancy, and R B Ashman
March 1984, Journal of the American Dental Association (1939),
C S Farah, and S Elahi, and K Drysdale, and G Pang, and T Gotjamanos, and G J Seymour, and R L Clancy, and R B Ashman
June 2003, Clinical evidence,
C S Farah, and S Elahi, and K Drysdale, and G Pang, and T Gotjamanos, and G J Seymour, and R L Clancy, and R B Ashman
June 2002, Clinical evidence,
C S Farah, and S Elahi, and K Drysdale, and G Pang, and T Gotjamanos, and G J Seymour, and R L Clancy, and R B Ashman
June 2005, Clinical evidence,
Copied contents to your clipboard!