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The next HLDA Workshop, HLDA9, will be Chaired by Pablo Engel, Immunology Unit. Department Cellular Biology and Pathology. Medical School; University of Barcelona. Casanova 143. Barcelona E-08036; e-mail: pengel@ub.edu

The Workshop studies will be carried out over the next two years. The results will be presented at a Conference to be held in Barcelona at the end of 2009. This Conference, tentatively titled “B cell targeting”, will focus on B cell biology and will also serve as a forum to discuss the use of monoclonal antibodies for the diagnosis and treatment of B cell-related diseases.

Data, both from the last workshop (HLDA8) and from analyses of the human genome, indicate that a large number of B cell-associated molecules have yet to be characterized. Examples include receptors of the Fc homologue family and the high number of as yet uncharacterized 4TM members.


Goals of the Workshop

The aim of this workshop, as with previous HLDA Workshops, is to provide an invaluable and ongoing service to the scientific community.

HLDA9 will study a panel of monoclonal antibodies against B cell-associated molecules. Only monoclonal antibodies against known cloned molecules will be included in the panel. Thus, no unknown antibody blind panels will be carried out. Some antibodies against known CD molecules expressed on B cells will also be included in this panel. MAbs will be provided by both researches and companies.

  1. Determine the reactivity of the mAbs on normal B cells and B cell malignancies.
  2. Defining new B cell subsets.
  3. Determining the expression of the B-cell associated molecules on other hematopoietic and non-hematopoietic cells.
  4. Identification and expression of intracellular molecules or epitopes of B cell associated molecules.
  5. Study of phospho-epitopes and other intracellular signaling molecules such as adapter molecules
  6. Determine the triggered activation/apoptosis induced by therapeutic mAbs, particularly chimeric/ humanised/human mAbs

Sections (updated)

The Workshop studies will be coordinated by four chairpersons, each responsible for a section.
For more details on the sections and how you can contribute, click on the links below (opens a new tab).

  1. Normal B cell and B cell subsets (FACS analysis).
  2. B-cell malignancies (FACS analysis): Chairman Dr. Valter Gattei (Italy).
  3. Immunohistochemical analysis of normal and malignant cells.
  4. Intracellular signaling molecules (FACS analysis and immunohistology).

We want to get as many international research groups involved as possible to generate high quality expression data for all the submitted antibodies.

Subsections

  1. TNFSF and TNFRSF molecules and B cells.
  2. Fc-receptor homologues on B cells.
  3. SLAMF molecules on B cells.
  4. Innate immunity receptors on B cells.
  5. Molecules on dendritic cells and B cells.
  6. Myeloma and plasma cells
  7. Ectodomain molecules and B cells

Conference

This conference should attract the interest of scientists working in the field of cell-surface molecules at all levels, from basic research to the development of antibodies for therapy. It should also attract the growing number of companies that sell antibodies for research and diagnosis, and which are now developing new technologies such as antibody and tissue arrays or signaling pathway arrays.

The Conference will focus on the following issues:

  • B cell Biology. B cell development. B cell activation. B cell differentiation and plasma cells. Memory.
  • Role of B cell in pathology. Diagnostic and therapy using mAbs against B-cell-associated molecules. B-cells in autoimmunity. B cell malignancies.
  • New techniques in the generation of antibodies. Human antibodies. Ontology of the development of antibodies for therapy.