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- Campath-1
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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/06/10 18:23:49」(JST)
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CD52 molecule |
Identifiers |
Symbols |
CD52 ; CDW52 |
External IDs |
OMIM: 114280 HomoloGene: 88652 GeneCards: CD52 Gene |
Gene ontology |
Cellular component |
• integral to plasma membrane
• membrane
• anchored to membrane
|
Biological process |
• elevation of cytosolic calcium ion concentration
• respiratory burst
|
Sources: Amigo / QuickGO |
|
Orthologs |
Species |
Human |
Mouse |
|
Entrez |
1043 |
n/a |
|
Ensembl |
ENSG00000169442 |
n/a |
|
UniProt |
P31358 |
n/a |
|
RefSeq (mRNA) |
NM_001803 |
n/a |
|
RefSeq (protein) |
NP_001794 |
n/a |
|
Location (UCSC) |
Chr 1:
26.64 – 26.65 Mb |
n/a |
|
PubMed search |
[1] |
n/a |
|
|
CAMPATH-1 antigen, also known as cluster of differentiation 52 (CD52), is a glycoprotein that in humans is encoded by the CD52 gene.
CD52 is present on the surface of mature lymphocytes, but not on the stem cells from which these lymphocytes were derived. It also is found on monocytes[1] and dendritic cells.[2] Further, it is found within the male genital tract and is present on the surface of mature sperm cells. It is not found on resting T cells but is expressed on activated T cells.[3]
CD52 is a peptide of 12 amino acids, anchored to glycosylphosphatidylinositol (GPI). Since it is highly negatively charged and present on sperm cells and lymphocytes, it has been conjectured that its function is anti-adhesion, allowing cells to freely move around.[4]
CD52 binds the ITIM (Immunoreceptor tyrosine-based inhibitory motif)-bearing sialic acid-binding lectin SIGLEC10.
Clinical significance
It is associated with certain types of lymphoma.[5]
It is the protein targeted by alemtuzumab, a monoclonal antibody used for the treatment of chronic lymphocytic leukemia. A phase III trial into treatment of relapsing-remitting Multiple Sclerosis showed a reduction in relapse rate, but no statistically significant reduction in accumulated disability, when used as a first-line therapy.[6] However, a sister study looking at patients in whom relapses had occurred despite treatment with interferon beta or glatiramer demonstrated reduction in both relapse rate and accumulated disability. 20% patients randomised to interferon beta 1a had "sustained accumulation of disability" compared with 13% in the alemtuzumab group. .[7]
References
- ^ Buggins AG, Mufti GJ, Salisbury J, Codd J, Westwood N, Arno M, Fishlock K, Pagliuca A, Devereux S (September 2002). "Peripheral blood but not tissue dendritic cells express CD52 and are depleted by treatment with alemtuzumab". Blood 100 (5): 1715–20. PMID 12176892.
- ^ Ratzinger G, Reagan JL, Heller G, Busam KJ, Young JW (February 2003). "Differential CD52 expression by distinct myeloid dendritic cell subsets: implications for alemtuzumab activity at the level of antigen presentation in allogeneic graft-host interactions in transplantation". Blood 101 (4): 1422–9. doi:10.1182/blood-2002-04-1093. PMID 12393688.
- ^ authors = Clark and Cook|date = 2013
- ^ Hale G, Waldmann H (2000). "From Laboratory to Clinic : The Story of CAM PA TH-1". Methods Mol. Med. 40: 243–66. doi:10.1385/1-59259-076-4:243. PMID 21337094.
- ^ Piccaluga PP, Agostinelli C, Righi S, Zinzani PL, Pileri SA (April 2007). "Expression of CD52 in peripheral T-cell lymphoma". Haematologica 92 (4): 566–7. doi:10.3324/haematol.10767. PMID 17488672.
- ^ Coles AJ, Twyman CL, Arnold DL, Cohen JA, Confavreux C, Fox EJ, Hartung HP, Havrdova E, Selmaj KW, Weiner HL, Miller T, Fisher E, Sandbrink R, Lake SL, Margolin DH, Oyuela P, Panzara MA, Compston DA (November 2012). "Alemtuzumab for patients with relapsing multiple sclerosis after disease-modifying therapy: a randomised controlled phase 3 trial". Lancet 380 (9856): 1829–39. doi:10.1016/S0140-6736(12)61768-1. PMID 23122650. [unreliable medical source?]
- ^ Cohen, Jeffrey; Coles A; Arnold D (24 November 2012). "Alemtuzumab versus interferon beta 1a as first-line treatment for patients with relapsing-remitting multiple sclerosis: a randomised controlled phase 3 trial". The Lancet 380 (9856): 1819–1828. doi:10.1016/S0140-6736(12)61769-3. Retrieved 28 December 2012.
External links
- CD52 antigen at the US National Library of Medicine Medical Subject Headings (MeSH)
UpToDate Contents
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- 1. 肺移植後の免疫抑制の導入induction immunosuppression following lung transplantation [show details]
…Alemtuzumab (Campath-1H) is a humanized preparation of monoclonal rat antibodies directed toward the CD52 antigen that is present on virtually all lymphocytes (both T and B cells). Alemtuzumab leads to depletion …
- 2. ナチュラルキラー(NK)細胞大顆粒リンパ球性白血病natural killer nk cell large granular lymphocyte leukemia [show details]
…limited. One patient with symptomatic chronic NK lymphocytosis responded to treatment with the anti-CD52 monoclonal antibody, alemtuzumab . The farnesyltransferase inhibitor tipifarnib achieved no objective…
- 3. 大顆粒リンパ球性白血病の治療treatment of large granular lymphocyte leukemia [show details]
…or allogeneic HCT (5 and 10 patients, respectively) . The monoclonal antibody alemtuzumab targets CD52 expressed on the surface of T cell LGL leukemia . Case reports and small case series have demonstrated…
- 4. 成人T細胞性白血病/リンパ腫の臨床症状、病理学的特徴、および診断clinical manifestations pathologic features and diagnosis of adult t cell leukemia lymphoma [show details]
…CD8- . Rare cases are CD4-/CD8+ or CD4+/CD8+. CD25 is expressed in a majority of the cases , as is CD52 . Anaplastic large cell variants react with CD30, but are negative for ALK protein and lack rearrangements…
- 5. 大顆粒T細胞リンパ球性白血病の臨床症状、病理学的特徴、および診断clinical manifestations pathologic features and diagnosis of t cell large granular lymphocyte leukemia [show details]
…phenotype is often associated with mutation of STAT5B . A CD4-/CD8- phenotype has been rarely described. CD52 is also expressed on these cells. Killer immunoglobulin-like receptor (KIR, CD158) expression has…
English Journal
- Multiplex Genome-Edited T-cell Manufacturing Platform for "Off-the-Shelf" Adoptive T-cell Immunotherapies.
- Poirot L1, Philip B2, Schiffer-Mannioui C1, Le Clerre D1, Chion-Sotinel I1, Derniame S1, Potrel P1, Bas C1, Lemaire L1, Galetto R1, Lebuhotel C1, Eyquem J1, Cheung GW2, Duclert A1, Gouble A1, Arnould S1, Peggs K2, Pule M2, Scharenberg AM3, Smith J4.
- Cancer research.Cancer Res.2015 Sep 15;75(18):3853-64. doi: 10.1158/0008-5472.CAN-14-3321. Epub 2015 Jul 16.
- Adoptive immunotherapy using autologous T cells endowed with chimeric antigen receptors (CAR) has emerged as a powerful means of treating cancer. However, a limitation of this approach is that autologous CAR T cells must be generated on a custom-made basis. Here we show that electroporation of trans
- PMID 26183927
- Outcomes Associated with Steroid Avoidance and Alemtuzumab among Kidney Transplant Recipients.
- Serrano OK1, Friedmann P2, Ahsanuddin S3, Millan C1, Ben-Yaacov A4, Kayler LK5.
- Clinical journal of the American Society of Nephrology : CJASN.Clin J Am Soc Nephrol.2015 Sep 4. pii: CJN.12161214. [Epub ahead of print]
- BACKGROUND AND OBJECTIVES: Alemtuzumab is a humanized anti-CD52 monoclonal antibody used as induction in kidney transplantation (KTX) since 2003. Few studies have evaluated long-term outcomes of this agent or changes in outcomes over time.DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: A retrospe
- PMID 26342042
- Alemtuzumab treatment for Sézary syndrome: a single center experience.
- Novelli S1, García-Muret P, Sierra J, Briones J.
- The Journal of dermatological treatment.J Dermatolog Treat.2015 Sep 2:1-15. [Epub ahead of print]
- INTRODUCTION: Sézary syndrome (SS) is characterized by rapidly progressive disease and poor survival. Although there is no standard treatment for SS, allogeneic stem cell transplantation (alloSCT) is the only treatment available that may offer a long survival. Alemtuzumab, a humanized monoclonal an
- PMID 26329989
Japanese Journal
- Evi-1高発現AMLに対する免疫療法のターゲットとしてのCD52分子
- 不妊と免疫--その基礎と臨床 (特集 不妊診療のすべて)
Related Links
- CD52 is a protein present on the surface of mature lymphocytes, but not on the stem cells from which these lymphocytes were derived. It also is found in monocytes and dendritic cells. It is a glycosylphosphatidylinositol (GPI)-- anchored antigen ...
Related Pictures
★リンクテーブル★
[★]
- 英
- cluster of differentiation, CD
- Bリンパ球 CD10,CD19,CD20
- Tリンパ球 CD2,CD3,CD5,CD7
- 幹細胞 CD34
- 顆粒球 CD13,CD33
- 単球 CD14:LPSをリガンドとし、Toll-like receptorと共役して細胞内シグナルを伝達する分子。
- 巨核球 CD41(GpIIb),CD42(GpIb)
- NK細胞:CD16(IgGのFc部に対する受容体)、CD56(NCAM-I)
[★]
- 同
- Campath-1 H
- 同
- Campath-1 H
[★]
- 関
- P-Selectin
- 関
- P-Selectin
[★]
- 同
- Leucine-1
発現細胞
- 胸腺細胞、T細胞、B細胞のサブセット (IMM)
- 胸腺細胞、T細胞、NK細胞、B1(B細胞のsubpopulation) (WCH.31)
- 成熟T細胞、胸腺細胞、一部のB細胞(CD5陽性B細胞(B-1細胞)。脾臓等、異所由来(骨髄非依存性)のB細胞) (資料1)
- B細胞性白血病・リンパ腫(資料1)
分子量
別名
機能
- CD5に対するモノクローナル抗体を作用させると、細胞内のチロシンのリン酸化が起こり、T細胞が活性化する。ただし、抑制的に作用する経路にも作用するかもしれない(WCH.31)
- CD5+ B細胞は自己抗体を産生する(WCH.31)
- CD72はCD5にたいするcounter-receptorである(WCH.31)
臨床関連
参考
- http://www.srl.info/srlinfo/kensa_ref_CD/KENSA/SRL5039.htm
- http://www.bc-cytometry.com/Data/db_search/CD005.htm
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