Lymphoid organ development in rabbits: Major lymphocyte subsets

Developmental and Comparative Immunology

Volumn 31, Issue 6, 2007, Pages 632-644

  Jeklova, Edita ^a,b   Leva, Lenka ^a   Faldyna, Martin ^a,b  

^a VETERINARY RESEARCH INSTITUTE   (Czech Republic)

^b UNIVERSITY OF VETERINARY AND PHARMACEUTICAL SCIENCES   (Czech Republic)

Author keywords

CD4; CD8; Flow cytometry; Lagomorpha; Post natal development

Indexed keywords

B LYMPHOCYTE ANTIGEN; CD79A ANTIGEN; CROSS REACTING ANTIBODY; MONOCLONAL ANTIBODY;

ANTIGEN SPECIFICITY; ARTICLE; BLOOD; CD4 CD8 RATIO; CD4+ T LYMPHOCYTE; CD8+ T LYMPHOCYTE; COMPARATIVE STUDY; COMPARTMENT MODEL; CONTROLLED STUDY; FEMALE; FLOW CYTOMETRY; FREQUENCY ANALYSIS; LYMPHOCYTE SUBPOPULATION; LYMPHOID ORGAN; MALE; MESENTERY LYMPH NODE; NEWBORN; NONHUMAN; ORGANOGENESIS; POPLITEAL VEIN; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; RABBIT; SPLEEN;

ANIMALIA; LAGOMORPHA; ORYCTOLAGUS CUNICULUS;

EID: 33846201307     PISSN: 0145305X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dci.2006.10.002     Document Type: Article

References (72)

1. Gamboa D., and Miller J.N. Experimental neonatal syphilis, I: evidence of resistance to symptomatic infection in neonatal rabbits following intradermal inoculation with Treponema pallidum (Nichlos strain). Pediatr Res 18 10 (1984) 965-971
2. Dannenberg Jr. A.M. Delayed-type hypersensitivity and cell-mediated immunity in the pathogenesis of tuberculosis. Immunol Today 12 7 (1991) 228-233
3. - T cell receptor-γ/δ cells by in vitro transformation with human T lymphotropic virus-I. J Exp Med 178 4 (1993) 1337-1345
4. Filice G., Cereda P.M., and Varnier O.E. Infection of rabbits with human immunodeficiency virus. Nature 335 6188 (1988) 366-369
5. Jayo J.M., Schwenke D.C., and Clarkson T.B. Atherosclerosis research. In: Manning P.J., Ringler D.H., and Newcomer C.E. (Eds). The biology of the laboratory rabbit. 2nd ed (1994), Academic Press, San Diego 367-376
6. Peiffer R.L., Pohm-Thorsen L., and Corcoran K. Models in ophthalmology and vision research. In: Manning P.J., Ringler D.H., and Newcomer C.E. (Eds). The biology of the laboratory rabbit. 2nd ed (1994), Academic Press, San Diego 410-430
7. Mage R.G. Immunology of lagomorphs. In: Pastoret P.P., Griebel P., Bazin H., and Govaerts A. (Eds). Handbook of vertebrate immunology (1998), Academic Press, San Diego 223-260
8. Joling P., Bianchi A.T.J., Kappe A.L., and Zwart R.T. Distribution of lymphocyte subpopulations in thymus, spleen, and peripheral blood of specific pathogen free pigs from 1 to 40 weeks of age. Vet Immunol Immunopathol 40 2 (1994) 105-117
9. Sellon R.K., Levy J.K., Jordan H.L., Gebhard D.H., Tompkins M.B., and Tompkins W.A. Changes in lymphocyte subsets with age in perinatal cats: late gestation through eight weeks. Vet Immunol Immunopathol 53 1-2 (1996) 105-113
10. Wilson R.A., Zolnai A., Rudas P., and Frenyo L.V. T-cell subsets in blood and lymphoid tissues obtained from fetal calves, maturing calves, and adult bovine. Vet Immunol Immunopathol 53 1-2 (1996) 49-60
11. Faldyna M., and Toman M. The effect of age on the distribution of lymphocyte and neutrophil granulocyte subsets in the peripheral blood of dog. Vet Med-Czech 43 6 (1998) 193-199
12. Faldyna M., Leva L., Knotigova P., and Toman M. Lymphocyte subsets in peripheral blood of dogs-a flow cytometric study. Vet Immunol Immunopathol 82 1-2 (2001) 23-37
13. Faldyna M., Sinkora J., Knotigova P., Leva L., and Toman M. Lymphatic organ development in dogs: major lymphocyte subsets and activity. Vet Immunol Immunopathol 104 3-4 (2005) 239-247
14. Jasper P.J., Zhai S.K., Kalis S.L., Kingzette M., and Knight K.L. B lymphocyte development in rabbit: progenitor B cells and waning of B lymphopoiesis. J Immunol 171 12 (2003) 6372-6380
15. Knight K.L., and Crane M.A. Generating the antibody repertoire in rabbit. Adv Immunol 56 (1994) 179-218
16. Lanning D., Sethupathi P., Rhee K.J., Zhai S.K., and Knight K.L. Intestinal microflora and diversification of the rabbit antibody repertoire. J Immunol 165 4 (2000) 2012-2019
17. + B cells are preferentially expanded in rabbit appendix: the role of CD5 in B cell development and selection. Dev Comp Immunol 30 8 (2006) 711-722
18. Lanning D., Zhu X., Zhai S.K., and Knight K.L. Development of the antibody repertoire in rabbit: gut-associated lymphoid tissue, microbes, and selection. Immunol Rev 175 (2000) 214-228
19. Rhee K.J., Sethupathi P., Driks A., Lanning D.K., and Knight K.L. Role of commensal bacteria in development of gut-associated lymphoid tissues and preimmune antibody repertoire. J Immunol 172 2 (2004) 1118-1124
20. Rhee K.J., Jasper P.J., Sethupathi P., Shanmugam M., Lanning D., and Knight K.L. Positive selection of the peripheral B cell repertoire in gut-associated lymphoid tissues. J Exp Med 201 1 (2005) 55-62
21. Fujiwara S., Armstrong R.M., and Cinader B. Age and organ dependent variations in the number of thymus derived RTLA bearing cells. Immunol Commun 3 3 (1974) 275-284
22. De Smet W., Vaeck M., Smet E., Brys L., and Hamers R. Rabbit leukocyte surface antigens defined by monoclonal antibodies. Eur J Immunol 13 11 (1983) 919-928
23. Watkins J.R., McNicholas J.M., Loken M.R., and Knight K.L. Characterization of functionally distinct subpopulations of rabbit T lymphocytes. Immunology 53 4 (1984) 659-667
24. Kotani M., Yamamura Y., Tamatani T., Kitamura F., and Miyasaka M. Generation and characterization of monoclonal antibodies against rabbit CD4, CD5 and CD11a antigens. J Immunol Methods 157 1-2 (1993) 241-252
25. Tokarz-Deptula B., and Deptula W. Values of selected immune and haematological parameters in healthy rabbits. Pol J Vet Sci 8 2 (2005) 107-112
26. Jones M., Cordell J.L., Beyers A.D., Tse A.G.D., and Mason D.Y. Detection of T and B cells in many animal species using cross-reactive anti-peptide antibodies. J Immunol 150 12 (1993) 5429-5435
27. Saalmuller A., Lunney J.K., Daubenberger C., Davis W., Fischer U., Göbel T.W., et al. Summary of the animal homologue section of HLAD8. Cell Immunol 236 1-2 (2005) 51-58
28. Laird C.W., Fox R.R., Mitchell B.P., Blau E.M., and Schultz H.S. Effect of strain and age on same hematological parameters in the rabbits. Am J Physiol 218 6 (1970) 1613-1617
29. Bortolotti A., Castelli D., and Bonati M. Hematology and serum chemistry values of adult, pregnant and newborn New Zealand rabbits (Oryctolagus cuniculus). Lab Anim Sci 39 5 (1989) 437-439
30. Boersma W.J.A., Steinmeier F.A., and Haaijman J.J. Age-related changes in the relative numbers of Thy-1 and Lyt-2-bearing peripheral blood lymphocytes in mice: a longitudinal approach. Cell Immunol 93 2 (1985) 417-430
31. Heaton P.R., Blount D.G., Mann S.J., Devlin P., Koelsch S., Smith B.H.E., et al. Assessing age-related changes in peripheral blood leukocyte phenotypes in domestic shorthaired cats using flow cytometry. J Nutr 132 6, Suppl. 2 (2002) 1607S-1609S
32. Heaton P.R., Blount D.G., Devlin P., Koelsch S., Mann S.J., Smith B.H.E., et al. Assessing age-related changes in peripheral blood leukocyte phenotypes in Labrador retriever dogs using flow cytometry. J Nutr 132 6, Suppl. 2 (2002) 1655S-1657S
33. HogenEsch H., Thompson S., Dunham A., Ceddia M., and Hayek M. Effect of age on immune parameters and the immune response of dogs to vaccines: a cross-sectional study. Vet Immunol Immunopathol 97 1-2 (2004) 77-85
34. Blount D.G., Pritchard D.I., and Heaton P.R. Age-related alterations to immune parameters in Labrador retriever dogs. Vet Immunol Immunopathol 108 3-4 (2005) 399-407
35. Borghetti P., De Angelis E., Saleri R., Cavalli V., Cacchoioli A., Corradi A., et al. Peripheral T lymphocyte changes in neonatal piglets: relationship with growth hormone (GH), prolactin (PRL) and cortisol changes. Vet Immunol Immunopathol 110 1-2 (2005) 17-25
36. Aldhous M.C., Raab G.M., Doherty K.V., Mok J.Y., Bird A.G., and Froebel K.S. Age-related ranges of memory, activation, and cytotoxic markers on CD4 and CD8 cells in children. J Clin Immunol 14 5 (1994) 289-298
37. Miller R.A. The aging immune systems: primer and prospectus. Science 273 5271 (1996) 70-74
38. Petty R.E., and Hunt D.W.C. Neonatal dendritic cells. Vaccine 16 14-15 (1998) 1378-1382
39. Morein B., Abusugra I., and Blomqvist G. Immunity in neonates. Vet Immunol Immunopathol 87 3-4 (2002) 207-213
40. Holt P.G., and Jones C.A. The development of the immune system during pregnancy and early life. Allergy 55 8 (2000) 688-697
41. English R.V., Nelson P., Johnson C.M., Nasisse M., Tompkins W.A., and Tompkins M.B. Development of clinical disease in cats experimentally infected with feline immunodeficiency virus. J Infect Dis 170 3 (1994) 543-552
42. Tokarz-Deptula B., and Deptula W. Dynamic alterations in peripheral blood lymphocytes in rabbits experimentally infected with VHD (viral hemorrhagic disease) virus-Polish strain Kr-1. Pol J Vet Sci 6 3 (2003) 67-69
43. Amadori A., Zamarchi R., De Silvestro G., Forza G., Cavatton G., Danieli G.A., et al. Genetic control of the CD4/CD8 T-cell ratio in humans. Nat Med 1 12 (1995) 1279-1283
44. Kraal G., Weissman I.L., and Butcher E.C. Genetic control of T-cell subset representation in inbred mice. Immunogenetics 18 6 (1983) 585-592
45. Sim B.C., Aftahi N., Reilly C., Bogen B., Schwartz R.H., Gascoigne N.R., et al. Thymic skewing of the CD4/CD8 ratio maps the T-cell receptor α-chain locus. Curr Biol 8 12 (1998) 701-704
46. van Meerwijk J.P., Bianchi T., Marguerat S., and MacDonald H.R. Thymic lineage commitment rather than selection causes genetic variation in size of CD4 and CD8 compartments. J Immunol 160 8 (1998) 3649-3654
47. Damoiseaux J.G., Cautain B., Bernard I., Mas M., van Breda Vriesman P.J., Druet P., et al. A dominant role for thymus and MHC genes in determining the peripheral CD4/CD8T cell ratio in the rat. J Immunol 163 6 (1999) 2983-2989
48. Jimenez E., Vicente A., Sacedon R., Munoz J.J., Weinmaster G., Zapata A.G., et al. Distinct mechanisms contribute to generate and change the CD4:CD8 cell ratio during thymus development: a role for the Notch ligand, Jagged 1. J Immunol 166 10 (2001) 5898-5908
49. Hasserjian R.P., Aster J.C., Davi F., Weinberg D.S., and Sklar J. Modulated expression of notch 1 during thymocyte development. Blood 88 3 (1996) 970-976
50. Felli M.P., Maroder M., Mitsiadis T.A., Campese A.F., Bellavia D., Vacca A., et al. Expression pattern of Notch1, 2 and 3 and Jagged 1 and 2 in lymphoid and stromal thymus components: distinct ligand-receptor interactions in intrathymic T cell development. Int Immunol 11 7 (1999) 1017-1025
51. Erkeller-Yuksel F.M., Deneys V., Yuksel B., Hannet I., Hulstaert F., Hamilton C., et al. Age-related changes in human blood lymphocyte subpopulations. J Pediatr 120 2, Part 1 (1992) 216-222
52. Hulstaert F., Hannet I., Deneys V., Munhyeshuli V., Reichert T., De Bruyere M., et al. Age-related changes in human blood lymphocyte subpopulations, II: varying kinetics of percentage and absolute count measurements. Clin Immunol Immunopathol 70 2 (1994) 152-158
53. Globerson A., and Effros R.B. Ageing of lymphocytes and lymphocytes in the aged. Immunol Today 21 10 (2000) 515-521
54. Sell S. The rabbit immune system: characterization of cell surface markers and functional properties of rabbit lymphocytes. Mol Immunol 16 12 (1979) 1045-1058
55. McNicholas J.M., Raffeld M., Loken M.R., Reiter H., and Knight K.L. Monoclonal antibodies to rabbit lymphoid cells: preparation and characterization of a T-cell-specific antibody. Mol Immunol 18 9 (1981) 815-822
56. Vajdy M., Sethupathi P., and Knight K.L. Dependence of antibody somatic diversification on gut-associated lymphoid tissue in rabbits. J Immunol 160 6 (1998) 2725-2729
57. Saalmuller A., Reddehase M.J., Buhring H.J., Jonjic S., and Koszinowski U.H. Simultaneous expression of CD4 and CD8 antigens by a substantial proportion of resting porcine T lymphocytes. Eur J Immunol 17 9 (1987) 1297-1301
58. Zuckermann F.A. Extrathymic CD4/CD8 double positive T cell. Vet Immunol Immunopathol 72 1-2 (1999) 55-66
59. Saalmuller A., Werner T., and Fachinger V. T-helper cells from naive to committed. Vet Immunol Immunopathol 87 3-4 (2002) 137-145
60. Denyer M.S., Wileman T.E., Stirling C.M.A., Zuber B., and Takamatsu H.H. Perforin expression can define CD8 positive lymphocyte subsets in pigs allowing phenotypic and functional analysis of natural killer, cytotoxic T, natural killer T and MHC un-restricted cytotoxic T-cells. Vet Immunol Immunopathol 110 3-4 (2006) 279-292
61. Bonomo A., Kehn P., and Shevach E.M. Premature escape of double-positive thymocytes to the periphery of young mice: possible role in autoimmunity. J Immunol 152 4 (1994) 1509-1514
62. + T lymphocytes. J Immunol 168 10 (2002) 5005-5013
63. Mackay C.R., and Hein W.R. A large proportion of bovine T cells express the gamma delta T cell receptor and show a distinct tissue distribution and surface phenotype. Int Immunol 1 5 (1989) 540-545
64. Mackay C.R., Beya M.F., and Matzinger P. Gamma/delta T cells express a unique surface molecule appearing late during thymic development. Eur J Immunol 19 8 (1989) 1477-1483
65. Reddehase M.J., Saalmuller A., and Hirt W. γδ T-lymphocyte subsets in swine. Curr Top Microbiol Immunol 173 (1991) 113-117
66. Sowder J.T., Chen C.L., Ager L.L., Chan M.M., and Cooper M.D. A large subpopulation of avian T cells express a homologue of the mammalian T gamma/delta receptor. J Exp Med 167 2 (1988) 315-322
67. Groh V., Porcelli S., Fabbi M., Lanier L.L., Picker L.J., Anderson T., et al. Human lymphocytes bearing T cell receptor γδ are phenotypically diverse and evenly distributed throughout the lymphoid system. J Exp Med 169 4 (1989) 1277-1294
68. Itohara S., Nakanishi N., Kanagawa O., Kubo R., and Tonegawa S. Monoclonal antibodies specific to native murine T-cell receptor γδ: Analysis of γδ T cells during thymic ontogeny and in peripheral lymphoid organs. Proc Natl Acad Sci USA 86 13 (1989) 5094-5098
69. Isono T., Kim C.J., and Seto A. Sequence and diversity of rabbit T-cell receptor gamma chain genes. Immunogenetics 41 5 (1995) 295-300
70. Cho K.S., Zhai S.K., Esteves P.J., and Knight K.L. Characterization of the T-cell receptor gamma locus and analysis of the variable gene segment expression in rabbit. Immunogenetics 57 5 (2005) 352-363
71. Bucy R.P., Chen C.L., Cihak J., Losch U., and Cooper M.D. Avian T cells expressing gamma delta receptors localize in splenic sinusoids and the intestinal epithelium. J Immunol 141 7 (1988) 2200-2205
72. Cooper M.D., Chen C.L., Bucy R.P., and Thompson C.B. Avian T cell ontogeny. Adv Immunol 50 (1991) 87-117