Abstract

Simple SummaryThe treatment of chronic lymphocytic leukemia (CLL) is a rapidly evolving field; however, despite recent progress, CLL remains incurable. Different types of immunotherapy have emerged as therapeutic options for CLL, aiming to boost anti-tumor immune responses; that said, despite initial promising results, not all patients benefit from immunotherapy. Relevant to this, the tumor microenvironment (TME) in CLL has been proposed to suppress effective immune responses while also promoting tumor growth, hence impacting on the response to immunotherapy as well. T cells, in particular, are severely dysfunctional in CLL and cannot mount effective immune responses against the malignant cells. However, reinvigoration of their effector function is still a possibility under the proper manipulation and has been associated with tumor regression. In this contribution, we examine the current immunotherapeutic options for CLL in relation to well-characterized T cell defects, focusing on possible counteracts that enhance anti-tumor immunity through the available treatment modalities.In the past few years, independent studies have highlighted the relevance of the tumor microenvironment (TME) in cancer, revealing a great variety of TME-related predictive markers, as well as identifying novel therapeutic targets in the TME. Cancer immunotherapy targets different components of the immune system and the TME at large in order to reinforce effector mechanisms or relieve inhibitory and suppressive signaling. Currently, it constitutes a clinically validated treatment for many cancers, including chronic lymphocytic leukemia (CLL), an incurable malignancy of mature B lymphocytes with great dependency on microenvironmental signals. Although immunotherapy represents a promising therapeutic option with encouraging results in CLL, the dysfunctional T cell compartment remains a major obstacle in such approaches. In the scope of this review, we outline the current immunotherapeutic treatment options in CLL in the light of recent immunogenetic and functional evidence of T cell impairment. We also highlight possible approaches for overcoming T cell defects and invigorating potent anti-tumor immune responses that would enhance the efficacy of immunotherapy.

Highlights

  • Chronic lymphocytic leukemia (CLL) is a malignancy of mature, antigen-experiencedB cells with a distinct immunophenotype (CD5+ CD23+ sIglow ) [1]

  • Molecular cues support that the unique characteristics of the clonotypic B cell receptor immunoglobulin (BcR IG) strongly affect the intensity of downstream intracellular signaling cascades in chronic lymphocytic leukemia (CLL) cells, regulating their proliferation and survival, and, eventually, impacting on the clinical course

  • The former category is characterized by low tumor-specificity and consists of mainly overexpressed antigens on the malignant cells or antigens that are expressed upon malignant transformation, while the latter category includes high specificity antigens on malignant cells derived from genomic aberrations [70,71]

Read more

Summary

Introduction

Chronic lymphocytic leukemia (CLL) is a malignancy of mature, antigen-experienced. B cells with a distinct immunophenotype (CD5+ CD23+ sIglow ) [1]. Evidence of a sole driver lesion is lacking in the pathophysiology of CLL, the prognostic relevance of these aberrations is well established, with subgroups defined by a particular aberration displaying distinct clinical course and outcome [7,8]. Adding to this complex picture, epigenetic mechanisms seem to play a role in the natural history of CLL, with significant differences in methylation signatures reported for CLL cells versus normal B cells, as well as between different patients [2,9,10,11]. This concept of a supportive milieu that promotes leukemogenesis has revolutionized our knowledge on the mechanisms supporting CLL cell survival and expansion, whereas it has highlighted new therapeutic targets for CLL regression

The Tumor Microenvironment in Chronic Lymphocytic Leukemia
Immunotherapy in CLL
Anti-CD20 Monoclonal Antibodies
Immune-Checkpoint Inhibitors
Bispecific T Cell Engager Antibodies
Immunomodulatory Drugs
Active Immunotherapy
Vaccines
CAR-T Cells
Immunomodulation as an Off-Target Effect of B Cell Receptor Inhibitors
Why Does Immunotherapy Work for Some but Not All Patients?
Mobilization
Imbalances in T Cell Subpopulations and Functions
Defective Immune Synapse Formation
Functional Incapacitation as an Aspect of Terminal Differentiation?
Chronic antigenicinstimulation
Concluding
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call