Molecular Aspects in Chronic Lymphocytic Leukemia patients with Autoimmune Cytopenias: single center experience

Objective: Autoimmune cytopenia's, particularly autoimmune hemolytic anemia (AIHA) and immune thrombocytopenia (ITP), complicate up to 25% of chronic lymphocytic leukemia (CLL) patients. Their occurrence correlates with a more aggressive disease. AIHA and ITP are more frequently found in patien...

Full description

Bibliographic Details
Main Authors: Sanja Trajkova, Nevenka Ridova, Marija Popova Labacevska, Aleksandra Pivkova Veljanovska, Simona Stojanovska, Dushko Dukovski, Milche Cvetanoski, Lazar Cadievski, Bozidar Kocoski, Irina Panovska Stavridis
Format: Article
Language:English
Published: Elsevier 2022-10-01
Series:Hematology, Transfusion and Cell Therapy
Online Access:http://www.sciencedirect.com/science/article/pii/S2531137922013608
_version_ 1811204838103449600
author Sanja Trajkova
Nevenka Ridova
Marija Popova Labacevska
Aleksandra Pivkova Veljanovska
Simona Stojanovska
Dushko Dukovski
Milche Cvetanoski
Lazar Cadievski
Bozidar Kocoski
Irina Panovska Stavridis
author_facet Sanja Trajkova
Nevenka Ridova
Marija Popova Labacevska
Aleksandra Pivkova Veljanovska
Simona Stojanovska
Dushko Dukovski
Milche Cvetanoski
Lazar Cadievski
Bozidar Kocoski
Irina Panovska Stavridis
author_sort Sanja Trajkova
collection DOAJ
description Objective: Autoimmune cytopenia's, particularly autoimmune hemolytic anemia (AIHA) and immune thrombocytopenia (ITP), complicate up to 25% of chronic lymphocytic leukemia (CLL) patients. Their occurrence correlates with a more aggressive disease. AIHA and ITP are more frequently found in patients with unfavorable biological risk factors for CLL. B lymphocytes at CLL are responsible of pathogenic mechanisms, involving aberrant antigen presentation and cytokine production. The aim of this study was evaluation of autoimmune cytopenia's in chronic lymphocytic leukemia patients from Republic of North Macedonia in correlation with genetic structure of pathologic B lymphocyte. Methodology: This is a retrospective study of patients with CLL, diagnosed and followed in the period between January 2011 and January 2021. Individual data from 100 treatment naïve CLL patients were analyzed, and mutational status and configuration of IGHV-IGHD-IGHJ rearrangements and genetics were analyzed using reverse transcriptase– polymerase chain reaction (RT-PCR) and sequencing methodology at the center for bimolecular pharmaceutical analyses, faculty of pharmacy, Skopje, Republic of North Macedonia. Results: Our evaluation have shown that 10% of CLL patients had AIHA and 4% had ITP. Most of the patients with autoimmune cytopenias had unmuteted IGHV genes. The most frequently expressed IGHV subgroup was IGHV1-69 (71%), followed by IGHV3-13 and IGHV4-4 (14%). The genetic results presented unfavorable cytogenetics with 11q deletions and NOTHCH mutation. Conclusion: The results of our study are consistent with published studies with specific molecular signature.
first_indexed 2024-04-12T03:20:27Z
format Article
id doaj.art-29d731c23fe84acc90a95127e9ad6a4f
institution Directory Open Access Journal
issn 2531-1379
language English
last_indexed 2024-04-12T03:20:27Z
publishDate 2022-10-01
publisher Elsevier
record_format Article
series Hematology, Transfusion and Cell Therapy
spelling doaj.art-29d731c23fe84acc90a95127e9ad6a4f2022-12-22T03:49:54ZengElsevierHematology, Transfusion and Cell Therapy2531-13792022-10-0144S27Molecular Aspects in Chronic Lymphocytic Leukemia patients with Autoimmune Cytopenias: single center experienceSanja Trajkova0Nevenka Ridova1Marija Popova Labacevska2Aleksandra Pivkova Veljanovska3Simona Stojanovska4Dushko Dukovski5Milche Cvetanoski6Lazar Cadievski7Bozidar Kocoski8Irina Panovska Stavridis9University St.Cyril and Methodius, Skopje, Macedonia University Clinic for Hematology, Skopje, MacedoniaUniversity St.Cyril and Methodius, Skopje, Macedonia University Clinic for Hematology, Skopje, MacedoniaUniversity St.Cyril and Methodius, Skopje, Macedonia University Clinic for Hematology, Skopje, MacedoniaUniversity St.Cyril and Methodius, Skopje, Macedonia University Clinic for Hematology, Skopje, MacedoniaUniversity St.Cyril and Methodius, Skopje, Macedonia University Clinic for Hematology, Skopje, MacedoniaUniversity St.Cyril and Methodius, Skopje, Macedonia University Clinic for Hematology, Skopje, MacedoniaUniversity St.Cyril and Methodius, Skopje, Macedonia University Clinic for Hematology, Skopje, MacedoniaUniversity St.Cyril and Methodius, Skopje, Macedonia University Clinic for Hematology, Skopje, MacedoniaUniversity St.Cyril and Methodius, Skopje, Macedonia University Clinic for Hematology, Skopje, MacedoniaUniversity St.Cyril and Methodius, Skopje, Macedonia University Clinic for Hematology, Skopje, MacedoniaObjective: Autoimmune cytopenia's, particularly autoimmune hemolytic anemia (AIHA) and immune thrombocytopenia (ITP), complicate up to 25% of chronic lymphocytic leukemia (CLL) patients. Their occurrence correlates with a more aggressive disease. AIHA and ITP are more frequently found in patients with unfavorable biological risk factors for CLL. B lymphocytes at CLL are responsible of pathogenic mechanisms, involving aberrant antigen presentation and cytokine production. The aim of this study was evaluation of autoimmune cytopenia's in chronic lymphocytic leukemia patients from Republic of North Macedonia in correlation with genetic structure of pathologic B lymphocyte. Methodology: This is a retrospective study of patients with CLL, diagnosed and followed in the period between January 2011 and January 2021. Individual data from 100 treatment naïve CLL patients were analyzed, and mutational status and configuration of IGHV-IGHD-IGHJ rearrangements and genetics were analyzed using reverse transcriptase– polymerase chain reaction (RT-PCR) and sequencing methodology at the center for bimolecular pharmaceutical analyses, faculty of pharmacy, Skopje, Republic of North Macedonia. Results: Our evaluation have shown that 10% of CLL patients had AIHA and 4% had ITP. Most of the patients with autoimmune cytopenias had unmuteted IGHV genes. The most frequently expressed IGHV subgroup was IGHV1-69 (71%), followed by IGHV3-13 and IGHV4-4 (14%). The genetic results presented unfavorable cytogenetics with 11q deletions and NOTHCH mutation. Conclusion: The results of our study are consistent with published studies with specific molecular signature.http://www.sciencedirect.com/science/article/pii/S2531137922013608
spellingShingle Sanja Trajkova
Nevenka Ridova
Marija Popova Labacevska
Aleksandra Pivkova Veljanovska
Simona Stojanovska
Dushko Dukovski
Milche Cvetanoski
Lazar Cadievski
Bozidar Kocoski
Irina Panovska Stavridis
Molecular Aspects in Chronic Lymphocytic Leukemia patients with Autoimmune Cytopenias: single center experience
Hematology, Transfusion and Cell Therapy
title Molecular Aspects in Chronic Lymphocytic Leukemia patients with Autoimmune Cytopenias: single center experience
title_full Molecular Aspects in Chronic Lymphocytic Leukemia patients with Autoimmune Cytopenias: single center experience
title_fullStr Molecular Aspects in Chronic Lymphocytic Leukemia patients with Autoimmune Cytopenias: single center experience
title_full_unstemmed Molecular Aspects in Chronic Lymphocytic Leukemia patients with Autoimmune Cytopenias: single center experience
title_short Molecular Aspects in Chronic Lymphocytic Leukemia patients with Autoimmune Cytopenias: single center experience
title_sort molecular aspects in chronic lymphocytic leukemia patients with autoimmune cytopenias single center experience
url http://www.sciencedirect.com/science/article/pii/S2531137922013608
work_keys_str_mv AT sanjatrajkova molecularaspectsinchroniclymphocyticleukemiapatientswithautoimmunecytopeniassinglecenterexperience
AT nevenkaridova molecularaspectsinchroniclymphocyticleukemiapatientswithautoimmunecytopeniassinglecenterexperience
AT marijapopovalabacevska molecularaspectsinchroniclymphocyticleukemiapatientswithautoimmunecytopeniassinglecenterexperience
AT aleksandrapivkovaveljanovska molecularaspectsinchroniclymphocyticleukemiapatientswithautoimmunecytopeniassinglecenterexperience
AT simonastojanovska molecularaspectsinchroniclymphocyticleukemiapatientswithautoimmunecytopeniassinglecenterexperience
AT dushkodukovski molecularaspectsinchroniclymphocyticleukemiapatientswithautoimmunecytopeniassinglecenterexperience
AT milchecvetanoski molecularaspectsinchroniclymphocyticleukemiapatientswithautoimmunecytopeniassinglecenterexperience
AT lazarcadievski molecularaspectsinchroniclymphocyticleukemiapatientswithautoimmunecytopeniassinglecenterexperience
AT bozidarkocoski molecularaspectsinchroniclymphocyticleukemiapatientswithautoimmunecytopeniassinglecenterexperience
AT irinapanovskastavridis molecularaspectsinchroniclymphocyticleukemiapatientswithautoimmunecytopeniassinglecenterexperience