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TBCA  -  tubulin folding cofactor A

Gallus gallus

 
 
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Disease relevance of TBCA

  • Serum immunoglobulin M (IgM) levels were not significantly elevated in ALV congenitally infected chickens except in those animals that had been injected with influenza virus in CFA [1].
  • Autoimmune glomerulonephritis was induced in chickens by immunization with human, bovine, turkey or chicken glomeruli in CFA [2].
 

High impact information on TBCA

  • On a molar basis, OVA.TBhsp70 was several hundred times more effective than OVA peptide plus CFA in eliciting specific CD8(+) T cell responses [3].
  • When lymph node cells were assessed on day 7, antigen specific proliferation was similarly observed both in the mice immunized with IFA and CFA [4].
  • Immunoelectron microscopy of SEF17- mutants grown on CFA agar+0.001% Congo red demonstrated the elaboration of an as yet undefined fimbrial structure [5].
  • However, growth of SEF17- mutants at 25 degrees C on CFA agar supplemented with 0.001% Congo red resulted in partial recovery of the phenotype [5].
  • Comparison of the three maps showed that the CFA 3 genome was approximately 3.5 kb smaller than that of CFA 44 and CFA 40 [6].
 

Biological context of TBCA

  • It is suggested that one mechanism of controlling the presence of CFA 10 on pigeon RBC's may be developmental changes in gene expression mediated through the serum environment [7].
  • The antibody response to a "T-independent" antigen (B. abortus) is greatly increased by CFA in dysgammaglobulinemic chickens [8].
  • This size difference was discounted as a likely cause of the reduced pathogenicity of CFA 3 as the other mildly virulent virus, CFA 44, was the same size as the hypervirulent CFA 40 [6].
 

Anatomical context of TBCA

  • Unique combinations of the thirteen serologically detectable CFA determinants are expressed on erythroid and lymphoid cells of all avian species tested [9].
 

Associations of TBCA with chemical compounds

  • Sugar inhibition assays using monospecific antisera against CFA 10 verified both the galactose-like specificity of the determinant and the possible significance of an alpha- vs. beta-internal linkage [7].

References

  1. Hypergammaglobulinemia in chickens congenitally infected with an avian leukosis virus. Qualtiere, L.F., Meyers, P. J. Immunol. (1976) [Pubmed]
  2. Experimental autoimmune glomerulonephritis in chickens: I. Influence of source of antigen, dose and adjuvant. Chandra, M. Autoimmunity (1988) [Pubmed]
  3. The adjuvant effects of Mycobacterium tuberculosis heat shock protein 70 result from the rapid and prolonged activation of antigen-specific CD8+ T cells in vivo. Harmala, L.A., Ingulli, E.G., Curtsinger, J.M., Lucido, M.M., Schmidt, C.S., Weigel, B.J., Blazar, B.R., Mescher, M.F., Pennell, C.A. J. Immunol. (2002) [Pubmed]
  4. Induction of skewed Th1/Th2 T-cell differentiation via subcutaneous immunization with Freund's adjuvant. Shibaki, A., Katz, S.I. Exp. Dermatol. (2002) [Pubmed]
  5. SEF17 fimbriae are essential for the convoluted colonial morphology of Salmonella enteritidis. Allen-Vercoe, E., Dibb-Fuller, M., Thorns, C.J., Woodward, M.J. FEMS Microbiol. Lett. (1997) [Pubmed]
  6. Comparison by restriction enzyme analysis of three fowl adenoviruses of varying pathogenicity. Pallister, J.A., Sheppard, M. Vet. Microbiol. (1996) [Pubmed]
  7. Identification of a galactose-like component of a chicken onco-developmental antigen. Dietert, R.R., Lewin, H.A., Kass, L.B. J. Hered. (1981) [Pubmed]
  8. Attempts to localize the defect in dysgammaglobulinemia of UM-B19 chickens by studying the effect of immunomodulating substances on immunoglobulin and antibody production. Kühlmann-Rabens, I., Wanke, R., Storandt, F., Altmann, B., Lösch, U., Merkenschlager, M. Vet. Immunol. Immunopathol. (1987) [Pubmed]
  9. Chicken fetal antigen: example of an antigenically complex oncodevelopmental membrane glycoprotein. Sanders, B.G., Dietert, R.R., Kline, K., Dietert, M. Oncodev. Biol. Med. (1981) [Pubmed]
 
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