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University of Malta

Development of monoclonal antibodies targeting T cell coinhibitory proteins TIM-3 and TIM-4

Abstract

dc:description.abstract

Immune checkpoint inhibition (ICI) therapy uses antibodies to block checkpoint proteins from binding with their partner proteins to help overcome dysfunctional T cells and promote the recognition and elimination of tumour cells. The exploration of novel immune checkpoint targets, like T cell immunoglobulin mucin 3 and 4 (TIM-3 and TIM-4), stems from trying to improve the efficacy of ICI therapies (e.g. against cytotoxic T-lymphocyte antigen 4 (CTLA-4) and/or programmed cell death protein 1 (PD-1)) which are currently being used to treat certain cancers like breast, colon and lung cancer either as sole agents or in combination with other immune checkpoint inhibitors or alternative treatments. Targeting TIM-3 and TIM-4 may reverse immune tolerance and suppress tumour cell growth and migration but no effective TIM-4 inhibitors have been developed yet. In this study, monoclonal single chain variable fragment (scFv) antibodies against TIM-3-Fc and TIM-4 were identified using phage display biopanning which isolated antibodies from large immunoglobulin gene repertoires displayed on the surface of bacteriophages. Thirty monoclones from each of the polyclonal pools of anti-TIM-3-Fc and anti-TIM-4 scFv antibodies displayed on phages were picked for validation. Enzyme-linked immunosorbent assay was used to determine the specificity of the phage clones to the target proteins TIM-3-Fc and TIM-4 respectively versus non-target proteins severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike S1 and SARS-CoV-2 receptor-binding domain proteins respectively. This revealed 21 anti-TIM-3-Fc scFv antibody phage monoclones with affinity and specificity to TIM-3-Fc and 8 anti-TIM-4 scFv antibody phage monoclones binding with affinity and specificity to TIM-4. Finally, sanger sequencing was used to determine the DNA sequence of the antiTIM-3-Fc and anti-TIM-4 scFv antibodies and to compare the resulting amino acid sequences to confirm that different scFv antibodies were identified for TIM-3-Fc versus TIM-4.

Degree

thesis:*
Grantor dc:publisher.institution
University of Malta
Year dc:date.issued
2024

Subjects

dc:subject × 3

Rights

dc:rights
Statement dc:rights
  • info:eu-repo/semantics/openAccess
Language dc:language.iso
en

Identifiers

dc:identifier.*
Repository record dc:identifier.uri
https://www.um.edu.mt/library/oar/handle/123456789/129869
OAI identifier oai:identifier
oai:www.um.edu.mt:123456789/129869

Chain of custody

source
Harvested from
University of Malta
Base URL
www.um.edu.mt/library/oar/oai/request
Last updated
2026-07-27
Source record
OAI-PMH GetRecord
citation

Development of monoclonal antibodies targeting T cell coinhibitory proteins TIM-3 and TIM-4. University of Malta, 2024. https://www.um.edu.mt/library/oar/handle/123456789/129869