CD4-8- T-cells increase in MRL/lpr mice treated with thymic factors

M. Mattei, S. Bach, S. Di Cesare, M. Fraziano, R. Placido, F. Poccia, I. Sammarco, A. M. Moras, M. R. Bardone, V. Colizzi

Research output: Contribution to journalArticle

Abstract

The in vivo effect of thymic factors on immature lymphocytes was analysed in MRL/lpr mice. This strain carries a genetic defect that causes during their life cycle a block of T-cell differentiation and abnormal proliferation of CD4-8- (double-negative, DN) T-lymphocytes. In vivo administration of four preparations of thymic factors, thymopentin (TP-1), thymopoietin (TP-5), thymolymphotropin (TLT), and thymomodulin (TMD) into young (2-month-old) MRL/lpr mice induced a significant increase of DN T-cells both in the thymus and in the peripheral lymph nodes, with a concomitant decrease of double-positive (DP) T-cells in the thymus and of single-positive (SP) T-cells in the lymph nodes. The level of DNA fragmentation measured as propidium iodide fluorescence was increased in the thymus population of young mice and in the lymph node population of old mice treated with TLT. SCID mice transplanted with lymph node cells from MRL/lpr donors (MRL→SCID) developed graft versus host (GvH) reaction due to the activation of MRL CD8+ alloreactive T-cells. This model was used to analyse the effect of TMD/TLT in vivo on MRL cell proliferation and expansion; in fact, spleen cells from MRL→SCID mice after treatment with TMD/TLT showed an increased cell proliferation, and an expansion of DN T-cells with a concomitant decrease of SP cells (both CD4+ and CD8+ cells). Decreased SP cell numbers in this context could explain why TMD/TLT treatment of SCID mice engrafted with MRL cells increased their survival compared to untreated MRL→SCID mice.

Original languageEnglish
Pages (from-to)651-658
Number of pages8
JournalInternational Journal of Immunopharmacology
Volume16
Issue number8
DOIs
Publication statusPublished - 1994

Fingerprint

Inbred MRL lpr Mouse
T-Lymphocytes
Thymopentin
Lymph Nodes
Thymus Gland
SCID Mice
Thymopoietins
Cell Proliferation
Propidium
DNA Fragmentation
Life Cycle Stages
Population
Cell Differentiation
Spleen
Cell Count
Fluorescence
thymolymphotropin
Lymphocytes
Transplants
thymomodulin

Keywords

  • double-negative T-cells
  • MRL/lpr mice
  • thymic factors

ASJC Scopus subject areas

  • Immunology
  • Pharmacology

Cite this

CD4-8- T-cells increase in MRL/lpr mice treated with thymic factors. / Mattei, M.; Bach, S.; Di Cesare, S.; Fraziano, M.; Placido, R.; Poccia, F.; Sammarco, I.; Moras, A. M.; Bardone, M. R.; Colizzi, V.

In: International Journal of Immunopharmacology, Vol. 16, No. 8, 1994, p. 651-658.

Research output: Contribution to journalArticle

Mattei, M, Bach, S, Di Cesare, S, Fraziano, M, Placido, R, Poccia, F, Sammarco, I, Moras, AM, Bardone, MR & Colizzi, V 1994, 'CD4-8- T-cells increase in MRL/lpr mice treated with thymic factors', International Journal of Immunopharmacology, vol. 16, no. 8, pp. 651-658. https://doi.org/10.1016/0192-0561(94)90138-4
Mattei, M. ; Bach, S. ; Di Cesare, S. ; Fraziano, M. ; Placido, R. ; Poccia, F. ; Sammarco, I. ; Moras, A. M. ; Bardone, M. R. ; Colizzi, V. / CD4-8- T-cells increase in MRL/lpr mice treated with thymic factors. In: International Journal of Immunopharmacology. 1994 ; Vol. 16, No. 8. pp. 651-658.
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abstract = "The in vivo effect of thymic factors on immature lymphocytes was analysed in MRL/lpr mice. This strain carries a genetic defect that causes during their life cycle a block of T-cell differentiation and abnormal proliferation of CD4-8- (double-negative, DN) T-lymphocytes. In vivo administration of four preparations of thymic factors, thymopentin (TP-1), thymopoietin (TP-5), thymolymphotropin (TLT), and thymomodulin (TMD) into young (2-month-old) MRL/lpr mice induced a significant increase of DN T-cells both in the thymus and in the peripheral lymph nodes, with a concomitant decrease of double-positive (DP) T-cells in the thymus and of single-positive (SP) T-cells in the lymph nodes. The level of DNA fragmentation measured as propidium iodide fluorescence was increased in the thymus population of young mice and in the lymph node population of old mice treated with TLT. SCID mice transplanted with lymph node cells from MRL/lpr donors (MRL→SCID) developed graft versus host (GvH) reaction due to the activation of MRL CD8+ alloreactive T-cells. This model was used to analyse the effect of TMD/TLT in vivo on MRL cell proliferation and expansion; in fact, spleen cells from MRL→SCID mice after treatment with TMD/TLT showed an increased cell proliferation, and an expansion of DN T-cells with a concomitant decrease of SP cells (both CD4+ and CD8+ cells). Decreased SP cell numbers in this context could explain why TMD/TLT treatment of SCID mice engrafted with MRL cells increased their survival compared to untreated MRL→SCID mice.",
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AU - Mattei, M.

AU - Bach, S.

AU - Di Cesare, S.

AU - Fraziano, M.

AU - Placido, R.

AU - Poccia, F.

AU - Sammarco, I.

AU - Moras, A. M.

AU - Bardone, M. R.

AU - Colizzi, V.

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AB - The in vivo effect of thymic factors on immature lymphocytes was analysed in MRL/lpr mice. This strain carries a genetic defect that causes during their life cycle a block of T-cell differentiation and abnormal proliferation of CD4-8- (double-negative, DN) T-lymphocytes. In vivo administration of four preparations of thymic factors, thymopentin (TP-1), thymopoietin (TP-5), thymolymphotropin (TLT), and thymomodulin (TMD) into young (2-month-old) MRL/lpr mice induced a significant increase of DN T-cells both in the thymus and in the peripheral lymph nodes, with a concomitant decrease of double-positive (DP) T-cells in the thymus and of single-positive (SP) T-cells in the lymph nodes. The level of DNA fragmentation measured as propidium iodide fluorescence was increased in the thymus population of young mice and in the lymph node population of old mice treated with TLT. SCID mice transplanted with lymph node cells from MRL/lpr donors (MRL→SCID) developed graft versus host (GvH) reaction due to the activation of MRL CD8+ alloreactive T-cells. This model was used to analyse the effect of TMD/TLT in vivo on MRL cell proliferation and expansion; in fact, spleen cells from MRL→SCID mice after treatment with TMD/TLT showed an increased cell proliferation, and an expansion of DN T-cells with a concomitant decrease of SP cells (both CD4+ and CD8+ cells). Decreased SP cell numbers in this context could explain why TMD/TLT treatment of SCID mice engrafted with MRL cells increased their survival compared to untreated MRL→SCID mice.

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