Target intelligence / Profile preview

Lymphocyte antigen CD52 (CD52)

Target
CD52
Molecular classification
Other, Receptor, Cell-surface glycoprotein, GPI-anchored protein
01

Overview

Lymphocyte antigen CD52 is a small, highly glycosylated, glycosylphosphatidylinositol-anchored cell-surface glycoprotein abundantly expressed on mature lymphocytes and also present on monocytes and dendritic cells, with lower levels on neutrophils and little to no expression on hematopoietic stem cells; it is also produced in the male genital tract and present on mature sperm cells. CD52’s exact physiological role is not fully defined; evidence supports roles in lymphocyte transendothelial migration, T-cell costimulation/activation, potential anti-adhesion properties, and interaction with the inhibitory lectin receptor SIGLEC10 via its ITIM pathway. Clinically, CD52 is an established therapeutic target: the humanized anti-CD52 antibody alemtuzumab depletes CD52-positive lymphocytes via ADCC and CDC and is used in chronic lymphocytic leukemia, in multiple sclerosis (relapsing–remitting) as immune reconstitution therapy, and in transplantation settings for lymphocyte depletion, with ongoing exploration in other hematologic malignancies (e.g., certain T/NK-cell neoplasms and FLT3-ITD–associated leukemias). Because CD52 expression can vary across diseases and patients, flow cytometric assessment of surface CD52 is recommended before initiating anti-CD52 therapy and can be used to monitor therapeutic targeting.

Other names
CAMPATH-1 antigenCluster of differentiation 52CAMPATH-1CD52 antigen
02

Mechanism of action

Antibody-dependent cellular cytotoxicity (ADCC) against CD52-positive cells; Complement-dependent cytotoxicity (CDC); Antibody-mediated lymphocyte depletion leading to immunosuppression

03

Biological functions

Immune responseLymphocyte transendothelial migrationT-cell costimulation/activationAnti-adhesion/anti-aggregation on immune cells and spermCell–cell interaction via SIGLEC10 binding
04

Disease associations

CancerInfectionInflammationAutoimmune diseaseHematologic malignancy (e.g., CLL, T/NK-cell lymphomas)Multiple sclerosisGraft-versus-host disease context (lymphocyte depletion)
05

Safety considerations

Infusion reactions from cytokine releaseProfound lymphocyte depletion causing infectionsSecondary autoimmunityCytopeniasCancer riskNeed for pre-therapy CD52 expression testing due to variable target expression
06

Interacting drugs

Alemtuzumab (anti-CD52 monoclonal antibody; Campath, Lemtrada)

1 more in the full profile.

07

Biomarkers

CD52 cell-surface expression by flow cytometry to select candidates for anti-CD52 therapy and to monitor responseAntigen density of CD52 on tumor/immune subsets

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