Relation between phenotype of tumor cells and clinicopathology in bovine leukosis.

Thirty-three cases of enzootic bovine leukosis (EBL) and 14 cases of sporadic bovine leukosis (SBL) were examined by immunohistochemistry using 6 monoclonal antibodies against leukocyte differentiation molecules of bovine leukocytes. There were 17 cases of B-1a cell type, 10 cases of B-1b cell type and 6 cases of B-2 cell type in EBL, and 5 cases originating from B cells (B-2 cell type) and 9 cases originating from immature T cells in SBL. The average age for the EBL cases of B-1a cell type was 8.6 years, B-1b cell type was 6.5 years, and of B-2 cell type was 4.5 years. In cases of SBL, immature T cell type patients were younger than B-2 cell type ones. The lymphoma originating from B cells differed from that originating from T cells in morphology. In T cell tumors, the nucleus of tumor cells was round, the edge of the cytoplasm obvious, and tumor cells were sporadically present and proliferated. When compared with T cells, the region among B cells was obscure. But, there was no relation between phenotype and the histologic classification of tumor cells. In EBL, beyond the lymph node, tumors of B-1a and B-1b types had developed in the heart and abomasum, and those of the B-2 type tended to occur in liver. In SBL, B-2 type and T type cells formed tumors in the liver, kidney, thymus, and one case of T-cell type tumor formed on the skin. We would like to propose a new classification of bovine leukosis as EBL, calf type B-cell lymphoma, juvenile T-cell lymphoma and skin type T-cell lymphoma.

[1]  L. Herzenberg,et al.  An unbiased analysis of V(H)-D-J(H) sequences from B-1a, B-1b, and conventional B cells. , 1997, Journal of immunology.

[2]  N. Ishiguro,et al.  The proto-oncogene c-myb is expressed in sporadic bovine lymphoma, but not in enzootic bovine leukosis. , 1996, The Journal of veterinary medical science.

[3]  Y. Aida,et al.  B-1a, B-1b and conventional B cell lymphoma from enzootic bovine leukosis. , 1996, Veterinary immunology and immunopathology.

[4]  H. Ungar-Waron,et al.  Detrimental effect of bovine leukemia virus (BLV) on the immunological state of cattle. , 1996, Veterinary immunology and immunopathology.

[5]  M. Bayık,et al.  Variable expression of CD49d antigen in B cell chronic lymphocytic leukemia is related to disease stages. , 1996, Leukemia.

[6]  Y. Aida,et al.  Phenotypic Analysis of Neoplastic Cells from Calf, Thymic, and Intermediate Forms of Bovine Leukosis , 1995, Veterinary pathology.

[7]  N. Ishiguro,et al.  Putative bovine B cell lineage tumor in sporadic bovine leukosis. , 1994, Veterinary immunology and immunopathology.

[8]  M. Tsudo,et al.  Differential expression of interleukin‐2 receptors (α and β chain) in mature lymphoid neoplasms , 1994 .

[9]  B. Polack,et al.  In vivo leukocyte tropism of bovine leukemia virus in sheep and cattle , 1994, Journal of virology.

[10]  W. Davis,et al.  Enhanced B-lymphocyte expression of IL-2R alpha associated with T lymphocytosis in BLV-infected persistently lymphocytotic cows. , 1994, Leukemia.

[11]  H. Ikematsu,et al.  Surface phenotype and Ig heavy-chain gene usage in chronic B-cell leukemias: expression of myelomonocytic surface markers in CD5- chronic B-cell leukemia , 1994 .

[12]  M. Hamilton,et al.  Identification of a monoclonal antibody reactive with the bovine orthologue of CD3 (BoCD3). , 1993, Veterinary immunology and immunopathology.

[13]  P. Youinou,et al.  CD5+ B cells and the immune system. , 1993, Immunology letters.

[14]  P. Casali,et al.  Autoimmunity-prone B-1 (CD5 B) cells, natural antibodies and self recognition. , 1993, Autoimmunity.

[15]  Diana J L Williams,et al.  Characterization and measurement of CD5+ B cells in normal and Trypanosoma congolense‐infected cattle , 1992, European journal of immunology.

[16]  L. Herzenberg,et al.  Characteristics and Development of the Murine B‐lb (Ly‐1 B Sister) Cell Population , 1992, Annals of the New York Academy of Sciences.

[17]  L. Herzenberg,et al.  Differential development of progenitor activity for three B-cell lineages. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[18]  J. Letesson,et al.  CD5+ B cells from bovine leukemia virus infected cows are activated cycling cells responsive to interleukin 2. , 1992, Leukemia.

[19]  A. Dang,et al.  Regulatory aspects of clonally expanded B-1 (CD5+B) cells , 1992, International journal of clinical & laboratory research.

[20]  A. Burny,et al.  FACS analysis of bovine leukemia virus (BLV)-infected cell lines with monoclonal antibodies (mAbs) to B cells and to monocytes/macrophages. , 1991, Veterinary immunology and immunopathology.

[21]  A. Burny,et al.  Bovine leukemia virus (BLV)-infected B-cells express a marker similar to the CD5 T cell marker. , 1989, Immunology letters.

[22]  P. Sopp,et al.  Two monoclonal antibodies (CC17, CC29) recognizing an antigen (Bo5) on bovine T lymphocytes, analogous to human CD5. , 1988, Veterinary immunology and immunopathology.

[23]  F. Sánchez‐Madrid,et al.  Co‐expression of Mac‐1 and p150,95 on CD5+ B cells. Structural and functional characterization in a human chronic lymphocytic leukemia , 1988, European journal of immunology.

[24]  R. Hardy,et al.  Normal, autoimmune, and malignant CD5+ B cells: the Ly-1 B lineage? , 1988, Annual review of immunology.

[25]  D. Baltimore,et al.  Depletion of the predominant B-cell population in immunoglobulin µ heavy-chain transgenic mice , 1987, Nature.

[26]  H. Lewin,et al.  The development and analysis of species specific and cross reactive monoclonal antibodies to leukocyte differentiation antigens and antigens of the major histocompatibility complex for use in the study of the immune system in cattle and other species. , 1987, Veterinary immunology and immunopathology.

[27]  G. Inghirami,et al.  Human lymphocytes making rheumatoid factor and antibody to ssDNA belong to Leu-1+ B-cell subset. , 1987, Science.

[28]  Y. Ikawa,et al.  No Involvement of Bovine Leukemia Virus in Sporadic Bovine Lymphosarcoma , 1986, Microbiology and immunology.

[29]  L Perelmutter,et al.  IgG4 and the immune system , 1983, Clinical reviews in allergy.

[30]  S. Numakunai,et al.  Pathologic studies on juvenile bovine leukosis. , 1980, Nihon juigaku zasshi. The Japanese journal of veterinary science.

[31]  I. Takashima,et al.  B-lymphocytes and T-lymphocytes in three types of bovine lymphosarcoma. , 1977, Journal of the National Cancer Institute.

[32]  A. Burny,et al.  Bovine leukemia virus: an exogenous RNA oncogenic virus. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[33]  Dungworth Dl,et al.  BOVINE LYMPHOSARCOMA IN CALIFORNIA. 3. THE CALF FORM. , 1965 .

[34]  Bendixen Hj Bovine enzootic leukosis. , 1965 .

[35]  H. Bendixen Bovine enzootic leukosis. , 1965, Advances in veterinary science.

[36]  J. Lengyel,et al.  Bovine Lymphosarcoma in California II. The Thymic Form , 1964 .