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Induction of functional CD154 (CD40 ligand) in neonatal T cells by cAMP‐elevating agents
Author(s) -
Suárez A.,
Mozo L.,
Gayo A.,
Simó A.,
Gutiérrez C.
Publication year - 2000
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1046/j.1365-2567.2000.00051.x
Subject(s) - cd154 , ionomycin , cd40 , biology , forskolin , cord blood , antigen , endocrinology , medicine , immune system , t cell , lymphoblast , il 2 receptor , immunology , cytotoxic t cell , microbiology and biotechnology , stimulation , cell culture , biochemistry , genetics , in vitro
Summary A deficiency of neonatal T lymphocytes to express CD154 antigen in response to ionomycin and phorbol 12‐myrsistate 13‐acetate (PMA) stimulation or after CD3 cross‐linking has been described. In the present report we describe that CD45RA + newborn cells are able to synthesize and express CD154 at similar or even higher levels than adult cells in response to ionomycin and cAMP‐elevating agents which trigger the protein kinase A (PKA) ‐mediated metabolic pathway. Peak CD154 protein concentrations in newborn cells were found between 4 and 8 hr after stimulation with ionomycin and dibutyryl cAMP. These agents, however, did not induce expression of the early activation antigen CD69. Surface levels of CD154 did not correlate with specific mRNA concentration, indicating that dibutyryl cAMP up‐regulates CD154 by acting at a post‐transcriptional stage. The CD154 antigen induced by PKA activation of newborn cells was functional, since upon binding to CD40 on B lymphocytes in the presence of interleukin‐4 (IL‐4), it promoted immunoglobulin heavy‐class switching to IgE. We also found a different pattern of cytokine production between neonatal and adult CD4 + T cells. In response to ionomycin and dibutyryl cAMP, cord blood cells were more prone than adult lymphocytes to secrete the T helper type 2‐derived immunosuppressive cytokines IL‐4 and IL‐10. Taking into account that the feto–maternal environment is rich in cAMP‐elevating agents, the reduced risk of graft versus host disease associated with cord blood trasplantation, as compared with the risk with adult bone marrow cell transplants, may be due to the bias of neonatal cells to differentiate towards the T helper type 2 functional cell subset.