Human Colostrum T Lymphocytes and Their Effector Cytokines Actively Aid the Development of the Newborn Immune System

Author:

Ciardelli L.,Garofoli F.,Stronati M.1,Mazzucchelli I.2,Avanzini M.A.3,Figar T.1,Gasparoni A.4,De Silvestri A.5,Sabatino G.6,Chirico G.4

Affiliation:

1. Neonatology and Neonatal Intensive Care Unit, Fondazione IRCCS Policlinico San Matteo, Pavia

2. Department of Internal Medicine and Therapeutics, Section of Pharmacology, University of Pavia, Pavia

3. Research Laboratories, Pediatric Oncohematology, Fondazione IRCCS Policlinico San Matteo, Pavia

4. Neonatology and Neonatal Intensive Care Unit, Spedali Civili, Brescia

5. Biometric Unit, Fondazione IRCCS Policlinico San Matteo, Pavia

6. Neonatal Intensive Care Unit, University G. d'Annunzio, Chieti, Italy

Abstract

Colostrum contains soluble and cellular components, the latter mainly T lymphocytes. We expanded in vitro colostrum T lymphocytes (CoTL) to evaluate phenotype and capability of cytokine production. We also considered paired cord blood T-lymphocytes (CBTL) representing the newborn “virgin” immune system. CoTL showed memory phenotype while CBTL expressed mainly naïve phenotype. CoTL included a balanced percentage of helper and cytotoxic subsets. We observed higher percentages of IL-2 (p=0.003) and IL-4 (p=0.027) producing cells by helper rather than by cytotoxic T lymphocytes. The greatest percentage of IFN-γ producing cells was in cytotoxic cells (p=0.0048), while no difference was found for IL-10. Cord blood samples consisted of a statistically significant greater percentage of helper than cytotoxic cells (p<0.001), with a low percentage of cytokine producing cells, confirming the immaturity of the newborn's immune system. CBTL percentage of IL-2 producing cells was higher for helper than cytotoxic subset (p<0.001). We observed a greater percentage of IFN-γ (p=0.001), IL-4 (p=0.003) and IL-10 (p<0.001) producing cells by cytotoxic than helper T lymphocytes. CoTL demonstrated to protect the newborn through the mother's previous immune experience and to supply active cytokines, which can help the postnatal development of both T type 1/T type 2 response.

Publisher

SAGE Publications

Subject

Pharmacology,Immunology,Immunology and Allergy

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