Human leukocyte immunoglobulin-like receptors in health and disease
Open accessAbstract
Human leukocyte immunoglobulin (Ig)-like receptors (LILR) are a family of 11 innate immunomodulatory receptors, primarily expressed on lymphoid and myeloid cells. LILRs are either activating (LILRA) or inhibitory (LILRB) depending on their associated signalling domains (D). With the exception of the soluble LILRA3, LILRAs mediate immune activation, while LILRB1-5 primarily inhibit immune responses and mediate tolerance. Abnormal expression and function of LILRs is associated with a range of pathologies, including immune insufficiency (infection and malignancy) and overt immune responses (autoimmunity and alloresponses), suggesting LILRs may be excellent candidates for targeted immunotherapies. This review will discuss the biology and clinical relevance of this extensive family of immune receptors and will summarise the recent developments in targeting LILRs in disease settings, such as cancer, with an update on the clinical trials investigating the therapeutic targeting of these receptors.
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LILRB proteins are type I transmembrane receptors predominantly expressed on hematopoietic cells.
“The LILRB proteins are type I transmembrane receptors predominantly expressed on hematopoietic cells14–20.”
From Oligomeric cystatin C supports the immunosuppressive activity of myeloid cells through interaction with inhibitory receptors (2025) · cites this paper as [19]
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LILRB4 signalling in leukaemia cells mediates T cell suppression and tumour infiltration
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Zhang, C., He, Y., Liu, X., Xie, J., Fang, M., Yang, X., Huang, R., Lou, Q., Li, B., Gupta, A., et al. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02462-x · Cited by 2 · see citing works
- Authors
- Redondo-García, S., Barritt, C., Papagregoriou, C., Yeboah, M., Frendeus, B., Cragg, M. S., & Roghanian, A.
- Affiliations
- Southampton General Hospital (GB)
- Glasgow Royal Infirmary (GB)
- Corresponding author
- Roghanian, Ali
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2023-11-13
- Volume
- 14
- Pages
- 1282874-1282874
- ISSN
- 1664-3224 (ISSN-L)
- PMC
- PMC10679719
- OpenAlex
- W4388646676
- Cited by
- 53
- References
- 2
- Citations by year
- 2026: 24 · 2025: 16 · 2024: 13
- FWCI
- 1.47
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Immunology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- ePrints Soton (University of Southampton) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Cancer Research UK (DRCRPG‐May23/100001, 24721)
- University of Southampton
- Blood Cancer UK (14043)
- Directorate for Biological Sciences
- Medical Research Council
- Biotechnology and Biological Sciences Research Council
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Cell Function and Interaction
- Life Sciences › Immunology and Microbiology › Immunology › Reproductive System and Pregnancy
- Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
- Keywords
- leukocyte immunoglobulin-like receptors, innate immune receptors, immunomodulation, immune tolerance, autoimmunity, alloresponse, cancer immunotherapy, clinical trials
- MeSH terms
- Humans, Immunoglobulins, Leukocytes, Receptors, Immunologic, Myeloid Cells, Immunomodulation
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