SIRPA (CD172a) | CD molecules | IUPHAR Guide to IMMUNOPHARMACOLOGY

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SIRPA (CD172a)

  Target has curated data in GtoImmuPdb

Target id: 2942

Nomenclature: SIRPA (CD172a)

Family: CD molecules, Signal regulatory proteins

Annotation status:  image of a grey circle Awaiting annotation/under development. Please contact us if you can help with annotation.  » Email us

Gene and Protein Information
Species TM AA Chromosomal Location Gene Symbol Gene Name Reference
Human 1 504 20p13 SIRPA signal regulatory protein alpha
Mouse 1 513 2 F1; 2 63.19 cM Sirpa signal-regulatory protein alpha
Rat 1 509 3q36 Sirpa signal-regulatory protein alpha
Gene and Protein Information Comments
Details are provided for the shorter protein isoform (isoform 1) encoded by the human gene. Isofom 2 is the longer protein at 508 amino acids (see NP_001317657). For the mouse, we show isoform 3 peptide details.
Database Links
CATH/Gene3D
Ensembl Gene
Entrez Gene
Human Protein Atlas
KEGG Gene
OMIM
RefSeq Nucleotide
RefSeq Protein
UniProtKB
Wikipedia
Immunopharmacology Comments
SIRPα is an important inhibitory immune response regulator. It is expressed by a subset of intestinal dendritic cells (integrin CD103+ DCs) that are critical for maintaining intestinal (mucosal) immune system homeostasis. This subset of CD103+SIRPα+ DCs selectively activates Th17 cells and type 3 innate lymphoid cells (ILC3) [3,5]. Studies by Hansen et al. (2018) have shown that CD103+SIRPα+ DCs can be transformed in to pro-inflammatory cells via a process involving FcαRI co-stimulation-induced glycolytic reprogramming. This work shows how IgA-immune complexes in the human intestine can convert a tolerogenic milieu to a pro-inflammatory one, following exposure to environmental agents [2].

In the cancer setting, SIRPα expressed on immune cells binds to CD47 on tumour cells, which down-regulates myeloid lineage cellsincluding DCs, tumour-associated macrophages and myeloid-derived suppressor cells. Pharmacological agents which block the SIRPα/CD47 antiphagocytic axis are being investigated as potential immuno-oncology therapeutics which would act to promote immunosurveillance and increase phagocytosis of cancer cells by tumour associated macrophages (TAMs). Specifically, the anti-SIPRα monoclonal antibody BI765063 (formerly OSE-172) is in early stage development (OSE IMMUNOTherapeutics), and proof of concept has been demonstrated in in vivo models. Preclinical testing suggests that the therapeutic effect of BI765063 is observed in both monotherapy or when combined with other checkpoint inhibitors, or with immune system stimulators. Anti-CD47 antibodies are also in early stage development, as reported by Gholamin et al. (2017) [1].
A strategy that involves derivatizing a kinase inhibitor with a cholesterol anchor (in this case creating an analogue of the CSF1R inhibitor BLZ945) and assembling it in a supramolecular structure with a macrophage-targeting anti-SIRPα mAb (which blocks the SIRPα/CD47 anti-phagocytic signal that is exploited by some cancer cells to avoid immune destruction) has been reported to enhance phagocytosis and removal of melanoma cancer cells by tumour associated macrophages in vitro and in vivo [4].
Immuno Process Associations
Immuno Process:  Inflammation
GO Annotations:  Associated to 8 GO processes
GO:0035696 monocyte extravasation ISS
GO:0043312 neutrophil degranulation TAS
GO:0050728 negative regulation of inflammatory response IMP
GO:0050765 negative regulation of phagocytosis ISS
GO:0050766 positive regulation of phagocytosis IBA
GO:0050900 leukocyte migration TAS
GO:0071346 cellular response to interferon-gamma ISS
GO:1900016 negative regulation of cytokine production involved in inflammatory response ISS
Immuno Process:  Chemotaxis & migration
GO Annotations:  Associated to 5 GO processes
GO:0035696 monocyte extravasation ISS
GO:0050870 positive regulation of T cell activation IBA
GO:0050900 leukocyte migration TAS
GO:0071641 negative regulation of macrophage inflammatory protein 1 alpha production ISS
GO:0071650 negative regulation of chemokine (C-C motif) ligand 5 production ISS
Immuno Process:  Cellular signalling
GO Annotations:  Associated to 2 GO processes
GO:0043312 neutrophil degranulation TAS
GO:0050870 positive regulation of T cell activation IBA
Immuno Process:  Cytokine production & signalling
GO Annotations:  Associated to 13 GO processes
GO:0032649 regulation of interferon-gamma production IMP
GO:0032651 regulation of interleukin-1 beta production ISS
GO:0032675 regulation of interleukin-6 production ISS
GO:0032680 regulation of tumor necrosis factor production IGI
GO:0032688 negative regulation of interferon-beta production ISS
GO:0032715 negative regulation of interleukin-6 production ISS
GO:0032720 negative regulation of tumor necrosis factor production ISS
GO:0071346 cellular response to interferon-gamma ISS
GO:0071347 cellular response to interleukin-1 ISS
GO:0071349 cellular response to interleukin-12 IMP
GO:0071641 negative regulation of macrophage inflammatory protein 1 alpha production ISS
GO:0071650 negative regulation of chemokine (C-C motif) ligand 5 production ISS
GO:1900016 negative regulation of cytokine production involved in inflammatory response ISS
Immuno Process:  Immune regulation
GO Annotations:  Associated to 3 GO processes
GO:0050728 negative regulation of inflammatory response IMP
GO:0050870 positive regulation of T cell activation IBA
GO:1900016 negative regulation of cytokine production involved in inflammatory response ISS
Immuno Process:  T cell (activation)
GO Annotations:  Associated to 1 GO processes
GO:0050870 positive regulation of T cell activation IBA
General Comments
The SIPRα protein binding interaction with CD47 produces an antiphagocytic signal, that is often termed a 'don't eat me' signal.
This protein contains an immunoglobulin (Ig)-like domain that resembles the antibody variable domain, that has been coined the 'V-set domain'. The genes for all human V-set domain containing proteins are listed in HGNC gene group 590.

References

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1. Gholamin S, Mitra SS, Feroze AH, Liu J, Kahn SA, Zhang M, Esparza R, Richard C, Ramaswamy V, Remke M et al.. (2017) Disrupting the CD47-SIRPα anti-phagocytic axis by a humanized anti-CD47 antibody is an efficacious treatment for malignant pediatric brain tumors. Sci Transl Med, 9 (381). [PMID:28298418]

2. Hansen IS, Krabbendam L, Bernink JH, Loayza-Puch F, Hoepel W, van Burgsteden JA, Kuijper EC, Buskens CJ, Bemelman WA, Zaat SAJ et al.. (2018) FcαRI co-stimulation converts human intestinal CD103+dendritic cells into pro-inflammatory cells through glycolytic reprogramming. Nat Commun, 9 (1): 863. [PMID:29491406]

3. Joeris T, Müller-Luda K, Agace WW, Mowat AM. (2017) Diversity and functions of intestinal mononuclear phagocytes. Mucosal Immunol, 10 (4): 845-864. [PMID:28378807]

4. Kulkarni A, Chandrasekar V, Natarajan SK, Ramesh A, Pandey P, Nirgud J, Bhatnagar H, Ashok D, Ajay AK, Sengupta S. (2018) A designer self-assembled supramolecule amplifies macrophage immune responses against aggressive cancer. Nature Biomedical Engineering,.

5. Watchmaker PB, Lahl K, Lee M, Baumjohann D, Morton J, Kim SJ, Zeng R, Dent A, Ansel KM, Diamond B et al.. (2014) Comparative transcriptional and functional profiling defines conserved programs of intestinal DC differentiation in humans and mice. Nat. Immunol., 15 (1): 98-108. [PMID:24292363]

How to cite this page

CD molecules: SIRPA (CD172a). Last modified on 07/08/2019. Accessed on 22/10/2019. IUPHAR/BPS Guide to PHARMACOLOGY, http://www.guidetoimmunopharmacology.org/GRAC/ObjectDisplayForward?objectId=2942.