Abstract
The most recent Human Leucocyte Differentiation Antigen Workshop ("HLDA7") took place in 2000 in Harrogate, UK and the proceedings are about to be published (Leucocyte Typing VII). New Sections were introduced in this Workship (Dendritic cells, Stem/progenitor cells, Erythroid cells and Carbohydrate Structures) and monoclonal antibodies were selected for which at least some molecular data were already available (to avoid "blind" screening of reagents against known specificities). A total of more than 80 new CD specificifies were established (previously the average was less than 30 new CD specificities per Workshop) and these are listed in this article. There is already evidence for the existence of many new leucocyte surface molecules for study at the next HLDA Workshop (in Adelaide in 2004), and we have listed in this article a number of such potential CD candidates (identified following the production of monoclonal antibodies or via gene cloning). There are also today an increasing number of lineage- and/or stage-restricted leucocyte-associated molecules localised within the cell cytoplasm (or nucleus): they will certainly prove of intense in the future for many laboratories studying human haematopoietic cells (regardless of whether a new "intracellular CD" categorisation scheme is devised for such molecules).
| Original language | English (US) |
|---|---|
| Pages (from-to) | 425-430 |
| Number of pages | 6 |
| Journal | Tissue Antigens |
| Volume | 58 |
| Issue number | 6 |
| DOIs | |
| State | Published - 2001 |
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Keywords
- CD antigens
- HLDA Workshop
ASJC Scopus subject areas
- Immunology
- Cell Biology
Cite this
CD antigens 2001. / Mason, D. Y.; André, P.; Bensussan, A.; Buckley, C.; Civin, C.; Clark, E.; De Haas, M.; Goyert, S.; Hadam, M.; Hart, D.; Hořejší, V.; Meuer, S.; Morissey, J.; Schwartz-Albiez, R.; Shaw, S.; Simmons, D.; Uguccioni, M.; Van Der Schoot, E.; Viver, E.; Zola, H.
In: Tissue Antigens, Vol. 58, No. 6, 2001, p. 425-430.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - CD antigens 2001
AU - Mason, D. Y.
AU - André, P.
AU - Bensussan, A.
AU - Buckley, C.
AU - Civin, C.
AU - Clark, E.
AU - De Haas, M.
AU - Goyert, S.
AU - Hadam, M.
AU - Hart, D.
AU - Hořejší, V.
AU - Meuer, S.
AU - Morissey, J.
AU - Schwartz-Albiez, R.
AU - Shaw, S.
AU - Simmons, D.
AU - Uguccioni, M.
AU - Van Der Schoot, E.
AU - Viver, E.
AU - Zola, H.
PY - 2001
Y1 - 2001
N2 - The most recent Human Leucocyte Differentiation Antigen Workshop ("HLDA7") took place in 2000 in Harrogate, UK and the proceedings are about to be published (Leucocyte Typing VII). New Sections were introduced in this Workship (Dendritic cells, Stem/progenitor cells, Erythroid cells and Carbohydrate Structures) and monoclonal antibodies were selected for which at least some molecular data were already available (to avoid "blind" screening of reagents against known specificities). A total of more than 80 new CD specificifies were established (previously the average was less than 30 new CD specificities per Workshop) and these are listed in this article. There is already evidence for the existence of many new leucocyte surface molecules for study at the next HLDA Workshop (in Adelaide in 2004), and we have listed in this article a number of such potential CD candidates (identified following the production of monoclonal antibodies or via gene cloning). There are also today an increasing number of lineage- and/or stage-restricted leucocyte-associated molecules localised within the cell cytoplasm (or nucleus): they will certainly prove of intense in the future for many laboratories studying human haematopoietic cells (regardless of whether a new "intracellular CD" categorisation scheme is devised for such molecules).
AB - The most recent Human Leucocyte Differentiation Antigen Workshop ("HLDA7") took place in 2000 in Harrogate, UK and the proceedings are about to be published (Leucocyte Typing VII). New Sections were introduced in this Workship (Dendritic cells, Stem/progenitor cells, Erythroid cells and Carbohydrate Structures) and monoclonal antibodies were selected for which at least some molecular data were already available (to avoid "blind" screening of reagents against known specificities). A total of more than 80 new CD specificifies were established (previously the average was less than 30 new CD specificities per Workshop) and these are listed in this article. There is already evidence for the existence of many new leucocyte surface molecules for study at the next HLDA Workshop (in Adelaide in 2004), and we have listed in this article a number of such potential CD candidates (identified following the production of monoclonal antibodies or via gene cloning). There are also today an increasing number of lineage- and/or stage-restricted leucocyte-associated molecules localised within the cell cytoplasm (or nucleus): they will certainly prove of intense in the future for many laboratories studying human haematopoietic cells (regardless of whether a new "intracellular CD" categorisation scheme is devised for such molecules).
KW - CD antigens
KW - HLDA Workshop
UR - http://www.scopus.com/inward/record.url?scp=18244409379&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=18244409379&partnerID=8YFLogxK
U2 - 10.1034/j.1399-0039.2001.580614.x
DO - 10.1034/j.1399-0039.2001.580614.x
M3 - Article
VL - 58
SP - 425
EP - 430
JO - HLA
JF - HLA
SN - 2059-2302
IS - 6
ER -