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Protein / target

B-cell receptor CD22

Encoded byCD22P20273Homo sapiensSwiss-Prot
Clinically validated
Therapeutic maturity
2
Approved medicines
Open Targets target-level
View by indication →
30
Clinical trials
Small-molecule tractable
Druggability
High-Quality Ligand

Protein at a glance

Biological role

Protein phosphatase binding

Strongest disease association

Precursor Cell Lymphoblastic Leukemia-Lymphoma

Via encoding gene CD22 · Clinical evidence · score 0.60

Therapeutic position

Established drug target

Antibodies

Research activity

Emerging research

4 papers · latest 2021

Derived from structured UniProt, Open Targets and literature data on this page.

Protein profile

UniProt 2026_02

Canonical identity and biological annotation from UniProt.

Function overview

Most highly expressed siglec (sialic acid-binding immunoglobulin-like lectin) on B-cells that plays a role in various aspects of B-cell biology including differentiation, antigen presentation, and trafficking to bone marrow.

View complete UniProt function annotation

Most highly expressed siglec (sialic acid-binding immunoglobulin-like lectin) on B-cells that plays a role in various aspects of B-cell biology including differentiation, antigen presentation, and trafficking to bone marrow (PubMed:34330755, PubMed:8627166). Binds to alpha 2,6-linked sialic acid residues of surface molecules such as CD22 itself, CD45 and IgM in a cis configuration. Can also bind to ligands on other cells as an adhesion molecule in a trans configuration (PubMed:20172905). Acts as an inhibitory coreceptor on the surface of B-cells and inhibits B-cell receptor induced signaling, characterized by inhibition of the calcium mobilization and cellular activation. Mechanistically, the immunoreceptor tyrosine-based inhibitory motif domain is phosphorylated by the Src kinase LYN, which in turn leads to the recruitment of the protein tyrosine phosphatase 1/PTPN6, leading to the negative regulation of BCR signaling (PubMed:8627166). If this negative signaling from is of sufficient strength, apoptosis of the B-cell can be induced (PubMed:20516366)

Subcellular location

Cell membrane
Domains and Gene Ontology detail (30)

Domains & features

Ig-like V-typeIg-like C2-type 1Ig-like C2-type 2Ig-like C2-type 3Ig-like C2-type 4Ig-like C2-type 5Ig-like C2-type 6

Gene Ontology

  • Ccell surface
  • Ccytoplasm
  • Cearly endosome
  • Cexternal side of plasma membrane
  • Cextracellular exosome
  • Cmembrane
  • Cneuronal cell body membrane
  • Cplasma membrane
  • Crecycling endosome
  • Fcarbohydrate binding
  • FCD4 receptor binding
  • FIgM binding

847 aa · 95 kDa · 5 isoforms

Biological roles

What this protein does, drawn together from its UniProt function, Gene Ontology terms and Reactome pathways.

Immune signallingUniProt · GO
View supporting evidence

Immune signalling

  • ·Most highly expressed siglec (sialic acid-binding immunoglobulin-like lectin) on B-cells…
  • ·B cell activation
  • ·negative regulation of B cell receptor signaling pathway
  • ·regulation of B cell proliferation

Concepts derived from UniProt GO Reactome — each badge above shows which sources supported that role.

Approved medicines with mapped indications

1 medicine · 3 areas

Approved therapies targeting this protein, grouped by what they are approved to treat — the disease-first view of the medicines below. Relationships come from the canonical approved-indication graph (ChEMBL phase-4), the same source as the drug cards.

Precursor B-Cell Lymphoblastic Leukemia-Lymphoma1 medicine
Precursor Cell Lymphoblastic Leukemia-Lymphoma1 medicine
Broader indication categories (1)
Neoplasms1 medicine

Broad umbrella indications (e.g. “Neoplasms”). Shown here because every medicine also appears under a more specific disease above — kept for completeness, de-emphasised for clarity.

2 medicines meet Open Targets' target-level approved-medicine definition; the 1 shown here are those on this page with a canonical approved disease indication in the graph. Approved indications from ChEMBL (phase-4), via the canonical drug→disease graph.

Drugs targeting this protein

1

How approved and investigational drugs engage this protein — mechanism and action type, direct vs complex targeting, and how broadly each acts across other targets. A drug-first view (the section above groups the approved ones disease-first); direct binders with few recorded targets are listed first.

inotuzumab ozogamicin
Narrow target profileApprovedBinding agent

CD22 binding agent

Indicated for Precursor B-Cell Lymphoblastic Leukemia-Lymphoma, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Neoplasms

Direct interaction with this protein · Only this protein recorded as a target

ChEMBL mechanism, action type, target identity and approved indications. Open Targets clinical status.

Translational evidence

Open Targets 26

Why this target matters therapeutically, strongest evidence first. Disease associations are gene-level (via the gene that encodes this protein) and open into the full confidence synthesis; the development universe, tractability and safety annotations are target-level, from Open Targets.

Strongest disease associations · via encoding gene CD22

Gene-level evidence surfaced through the gene CD22that encodes this protein — not a direct protein–disease relationship. Ranked by Forefront's causal-directness weighting, so genetically- and clinically-evidenced diseases lead over ones that merely share the literature.

Precursor Cell Lymphoblastic Leukemia-Lymphoma
0.74Moderately supported

Clinical evidence dominant · Open Targets 0.60

Neoplasms
0.63Moderately supported

Clinical evidence dominant · Open Targets 0.49

B-cell acute lymphoblastic leukemia
0.56Moderately supported

Clinical evidence dominant · Open Targets 0.45

Lupus Erythematosus, Systemic
0.52Moderately supported

Clinical evidence dominant · Open Targets 0.41

Lymphoma, Non-Hodgkin's
0.42Limited support

Clinical evidence dominant · Open Targets 0.32

View evidence synthesis (5)
Precursor Cell Lymphoblastic Leukemia-LymphomaModerately supported
0.74
agreement 0.590.90
Clinical84%Literature17%

Open Targets aggregate 0.60 · 2 independent evidence families

NeoplasmsModerately supported
0.63
agreement 0.470.78
Clinical81%Literature19%

Open Targets aggregate 0.49 · 2 independent evidence families

B-cell acute lymphoblastic leukemiaModerately supported
0.56
agreement 0.400.71
Clinical96%Literature5%

Open Targets aggregate 0.45 · 2 independent evidence families

Lupus Erythematosus, SystemicModerately supported
0.52
agreement 0.360.68
Clinical89%Literature11%

Open Targets aggregate 0.41 · 2 independent evidence families

Lymphoma, Non-Hodgkin'sLimited support
0.42
agreement 0.260.57
Clinical89%Literature11%

Open Targets aggregate 0.32 · 2 independent evidence families

The evidence agreement range shows how closely the independent evidence families agree — it is not a statistical confidence interval, and nothing here is fitted to outcome data. Derived from Open Targets evidence types under Forefront weighting; the per-type scores above show the calculation.

Show all associations
Precursor Cell Lymphoblastic Leukemia-Lymphoma0.60
Neoplasms0.49
B-cell acute lymphoblastic leukemia0.45
Lupus Erythematosus, Systemic0.41
Lymphoma, Non-Hodgkin's0.32
Lymphoma0.30
Lymphoma, Follicular0.30
Sjogren's Syndrome0.26

Drug development

11 compounds recorded · 2 approved · 9 in clinical development

Open Targets' development universe — every compound recorded against the target at any stage, not all approved medicines. Distinct from the 1 drug that targets this protein in Forefront's canonical graph (1 with a mapped approved indication, shown above): these count different sets and are not a subset relation.

View all recorded compounds (10)
INOTUZUMAB OZOGAMICINApproval
MOXETUMOMAB PASUDOTOXApproval
YTTRIUM Y 90 EPRATUZUMAB TETRAXETANPhase 2
BL22Phase 2
YTTRIUM Y 90 EPRATUZUMABPhase 1 2
MONO-DGA-RFB4Phase 1
EPRATUZUMABPhase 3
EPRATUZUMAB-CYS-TESIRINEPhase 1 2
BECTUMOMABPhase 3
INOTUZUMABPhase 3

Open Targets known-drugs universe. Drug name and highest clinical stage only — the disease relationship is NOT read from this slice (it carries trial-context noise); approved indications come from the canonical graph above.

Tractability

Small moleculesEmerging

Feasibility evidence (high-quality ligand) — no clinical-stage drug of this modality recorded.

AntibodiesStrong

Approved Drug and UniProt loc high conf support this modality.

Protein degradersEmerging

Feasibility evidence (database ubiquitination and half-life data) — no clinical-stage drug of this modality recorded.

Other modalitiesStrong

Approved Drug support this modality.

View underlying tractability evidence (9)
SM · High-Quality LigandAB · Approved DrugAB · UniProt loc high confAB · GO CC high confAB · UniProt SigP or TMHMMPR · Database UbiquitinationPR · Half-life DataPR · Small Molecule BinderOC · Approved Drug

Raw Open Targets tractability assessment buckets, by modality.

Clinical trials

30

Trials of drugs that target this protein — reached indirectly through those drugs, so a trial listed here studies the drug, not the protein. Ranked by active status, then clinical phase and recency, and spread across the targeting drugs.

View all trials (26)

RECRUITING · via inotuzumab ozogamicin · NCT03104491

TERMINATED · via inotuzumab ozogamicin · NCT03856216

ClinicalTrials.gov via the drug-target graph.

What's happening now

1

Recent therapeutic activity around this target — regulatory actions, clinical trials and safety signals for a drug that targets this protein, plus publications where such a drug is a genuine subject. Every item is reached indirectly through the drug, not the protein itself; incidental mentions (a paper that merely measures a drug) and press items are excluded.

  1. Regulatory approval2017-06-28

    Approval: Besponsa (EMA)

    ema · regulatory · ema · via inotuzumab ozogamicin

Objective event titles are shown unmodified; the event kind and significance line are derived from structured fields. Forefront AttentionEvent stream aggregating Europe PMC Regulatory filings ClinicalTrials.gov.

Research activity

4 papers · to 2021

Papers linked directly to this protein. This is the protein's own literature — descriptor-derived papers are kept separate below.

Most cited

Recent

Europe PMC papers linked directly to this protein.