(immunology) Glycoproteins that are expressed on the surface of immature thymocytes, Langerhans cells, and certain B cells, similar in structure to class I major histocompatibility complex molecules.
(immunology) Glycoproteins that are expressed on the surface of immature thymocytes, Langerhans cells, and certain B cells, similar in structure to class I major histocompatibility complex molecules.
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| Veterinary Dictionary: CD1 |
1. canine distemper.
2. curative dose; that which is sufficient to restore normal health.
| Wikipedia: CD1 |
| CD1a molecule | |
|---|---|
| Identifiers | |
| Symbol | CD1A |
| Alt. symbols | CD1 |
| Entrez | 909 |
| HUGO | 1634 |
| OMIM | 188370 |
| RefSeq | NM_001763 |
| UniProt | P06126 |
| Other data | |
| Locus | Chr. 1 q22-q23 |
| CD1b molecule | |
|---|---|
| Identifiers | |
| Symbol | CD1B |
| Alt. symbols | CD1 |
| Entrez | 910 |
| HUGO | 1635 |
| OMIM | 188360 |
| RefSeq | NM_001764 |
| UniProt | P29016 |
| Other data | |
| Locus | Chr. 1 q22-q23 |
| CD1c molecule | |
|---|---|
| Identifiers | |
| Symbol | CD1C |
| Alt. symbols | CD1 |
| Entrez | 911 |
| HUGO | 1636 |
| OMIM | 188340 |
| RefSeq | NM_001765 |
| UniProt | P29017 |
| Other data | |
| Locus | Chr. 1 q22-q23 |
| CD1d molecule | |
|---|---|
| Identifiers | |
| Symbol | CD1D |
| Entrez | 912 |
| HUGO | 1637 |
| OMIM | 188410 |
| RefSeq | NM_001766 |
| UniProt | P15813 |
| Other data | |
| Locus | Chr. 1 q22-q23 |
| CD1e molecule | |
|---|---|
| Identifiers | |
| Symbol | CD1E |
| Entrez | 913 |
| HUGO | 1638 |
| OMIM | 188411 |
| RefSeq | NM_030893 |
| UniProt | P15812 |
| Other data | |
| Locus | Chr. 1 q22-q23 |
CD1 (cluster of differentiation 1) is a family of glycoproteins expressed on the surface of various human antigen-presenting cells. They are related to the class I MHC molecules, and are involved in the presentation of lipid antigens to T cells. However their precise function is unknown.[1]
Contents |
CD1 glycoproteins can be classified primarily into two groups which differ in their lipid anchoring.[2]
CD1a, CD1b and CD1c (group 1 CD1 molecules) are expressed on cells specialized for antigen presentation.[3]
CD1d (group 2 CD1) is expressed in a wider variety of cells.
CD1e is an intermediate form, expressed intracellularly, the role of which is currently unclear.[4]
Group 1 CD1 molecules have been shown to present foreign lipid antigens, and specifically a number of mycobacterial cell wall components, to CD1-specific T cells.
The natural antigens of group 2 CD1 are not well-characterized, but a synthetic glycolipid, alpha-galactosylceramide, originally isolated from a compound found in a marine sponge, has strong biologic activity.
Group 2 CD1 molecules activate a group of T cells, known as Natural killer T cells because of their expression of NK surface markers such as CD161. Natural Killer T (NKT) cells are activated by CD1d-presented antigens, and rapidly produce Th1 and Th2 cytokines, typically represented by interferon-gamma and IL-4 production.
The group 2 (CD1d) ligand alpha-galactosylceramide is currently in phase I clinical trials for the treatment of advanced non-hematologic cancers.
Mice lack the group 1 CD1 molecules, and instead have 2 copies of CD1d. Thus, mice have been used extensively to characterize the role of CD1d and CD1d-dependent NKT cells in a variety of disease models.
It has recently been shown that cows lack the group 2 CD1 molecules, and have an expanded set of group 1 CD1 molecules.[5] Because of this and the fact that cows are a natural host of Mycobacterium bovis, a pathogen in humans as well, it is hoped that studying cows will yield insights into the group 1 CD1 antigen-presenting system.
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