Assessment of non-classical lymphocyte populations in patients with advanced lung cancer treated with Biomodulina T following platinum-based chemotherapy

Author:

Suárez Gisela María1ORCID,Catalá Mauricio2,Peña Yadira2,Portela Susana2,Añé-Kourí Ana Laura3ORCID,González Amnely3,Lorenzo-Luaces Patricia3ORCID,Díaz Manuel4,Molina María de los A.2,Pereira Karla3,Hernández Jenysbel de la C.3ORCID,Reyes Mary Carmen5ORCID,Ledón Nuris3ORCID,Mazorra Zaima1ORCID,Crombet Tania3ORCID,Lage Agustin3ORCID,Bencomo-Hernandez Antonio6ORCID,Saavedra Danay3ORCID

Affiliation:

1. Clinical Immunology Department, Center of Molecular Immunology, Havana 11600, Cuba; Laboratory of Immunology, Abu Dhabi Stem Cells Center, Abu Dhabi, United Arab Emirates

2. Oncology Unit, Medical & Surgical Research Center (CIMEQ), Havana 11300, Cuba

3. Clinical Immunology Department, Center of Molecular Immunology, Havana 11600, Cuba

4. Benéfico-Jurídico Pneumological Hospital, Havana 10600, Cuba

5. Clinical Direction, National Center for Biopreparations, Bejucal, Mayabeque 32600, Cuba

6. Laboratory of Immunology, Abu Dhabi Stem Cells Center, Abu Dhabi, United Arab Emirates

Abstract

Aim: Currently, malignant diseases represent a health issue worldwide. Among these, lung cancer is of growing importance, due to its high incidence and mortality. Chemotherapy, one of the most frequently used treatments, has shown its ability to induce accelerated immunosenescence in classic and as well non-classic lymphocyte compartments, being less described in the latter. The immune restoration strategies have demonstrated their ability to reverse immunosenescence and exhaustion markers in conventional lymphocyte subpopulations after chemotherapy. However, the possible immunorestorative effect on non-classical lymphocytes has not been widely reported. The aim of this study was to evaluate the effect of chemotherapy and the administration of a thymic polypeptide factor on non-classical lymphocyte populations in patients with advanced lung cancer. Methods: Eighteen patients with advanced lung cancer, were evaluated at baseline before and after platinum-based chemotherapy (4–6 cycles). All patients could complete treatment with a thymic polypeptide factor [Biomodulina T (BT)] at the end of chemotherapy. Blood from patients was collected by venipuncture in heparinized tubes before and after chemotherapy and at the end of BT treatment to analyze the frequencies of non-classical immune subpopulations by flow cytometry. Results: Natural killer (NK), natural killer T cells (NKT), and double-positive T lymphocyte (DPT) proportions reached normal values in patients diagnosed with advanced lung cancer before receiving cytotoxic treatment. Chemotherapy did not induce modifications in the total percent of NK, NKT, and DPT populations in these patients. However, the administration of BT decreased DPTs and NK cells expressing the cluster of differentiation (CD)57 molecule, which is considered a marker of immunosenescence. Conclusions: These results suggest a lower influence of platinum-based chemotherapy on non-classical lymphocytes and the potential to generate a reconstitution of lymphocyte subpopulations in patients with advanced lung cancer by using the thymic factor BT, which reveals a new possibility for improving the response to cancer immunotherapies [Cuban Public Registry of Clinical Trial (RPCEC, https://rpcec.sld.cu/en/trials/RPCEC00000358-En) identifier: RPCEC00000358].

Publisher

Open Exploration Publishing

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