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Method for the detection, preparation and depletion of cd4+ t lymphocytes

a technology of cd4+ t lymphocytes and t lymphocytes, which is applied in the field of synthetic peptides, can solve the problems of inefficient detection, unsatisfactory current methods to achieve these goals, and the detection tools still remain relatively inefficient, so as to increase the binding affinity of mhc-epitope complexes, increase the number and duration of dimer formation, and increase the number of synapse formation

Inactive Publication Date: 2016-03-31
IMCYSE
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent describes a way to make peptides that can be better recognized by the immune system, particularly by CD4+ T cells. This is done by adding a specific element called an oxidoreductase motif to the peptides. This makes it easier to detect and prepare specific T cells for use in diagnostic methods and in treating disease. The added motif makes the peptides better at binding to the MHC protein and this can lead to higher numbers and purity of CD4+ T cells being isolated.

Problems solved by technology

Current methods to achieve these goals are, however, unsatisfactory.
TCR low affinity results in inefficient detection, in particular in complex body fluids.
However, although both the specificity and sensitivity of these multimers have been significantly increased, these detection tools still remain relatively inefficient under circumstances of low T cell frequency or when TCR affinity is a limiting factor, such as for T cells in naïve configuration.
The contrast between the increasing need for methods to detect CD4+ T cells in areas as diverse as auto-immune diseases, cancer or evaluation of responses towards vaccination, to cite just a few, and the poor efficiency of available methods makes it an urgent need to improve such methods

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

Use of Tetramers of MHC Class II Molecules for the Detection of MOG-Specific CD4+ T Lymphocytes in the Naïve Human T Cell Repertoire

[0148]Multiple sclerosis is a chronic demyelination disease in which CD4+ T cells towards auto antigens such as the myelin oligodendrocytic glycoprotein (MOG) play a key role. The migration of effector cells through the brain-blood barrier elicits brain tissue destruction.

[0149]Such effector CD4+ T cells are generated from peripheral blood naïve T cells after cognate interaction with antigen-presenting cells presenting the MOG epitope within MHC class II complexes. Enumerating (i.e. identifying and quantifying) MOG-specific naïve CD4+ T cells is therefore predictive of disease outcome. However, the frequency of naïve T cell and affinity for MOG epitope are low, which prevents their detection by conventional technology, as for instance soluble tetramers of MHC class II molecules loaded with the MOG epitope.

[0150]One of such major MHC class II epitope of ...

example 2

Use of Tetramers of MHC Class II Molecules for the Follow-Up of Specific CD4+ T Cells During Vaccination and for Modulation of the Vaccination Strategy

[0154]The effectiveness of vaccination for infectious diseases depends on the number of CD4+ T cells which can be activated by such vaccination. An early and predictive sign of successful vaccination can be found in the increase in the number of vaccine-specific CD4+ T cells, a useful parameter to decide whether the vaccination strategy has to be modified by, for instance, increasing the number of vaccine administrations.

[0155]Influenza virus vaccination is a significant example in so far as there is only a loose correlation between the concentration of specific antibodies and the robustness of protection.

[0156]A major MHC class II-restricted epitope of the virus is located in the hemagglutinin protein. Peptide of sequence CGHCKYVKQNTLKHEMAGG (SEQ ID NO: 3 is therefore produced and loaded onto MHC class II tetramers as described in ex...

example 3

Depletion of Donor-Specific Specific CD4+ T Cells from the Host Repertoire to Improve Bone Marrow Grafting

[0161]Bone marrow rejection occurs when CD4+ T lymphocytes from the recipient react towards alloantigens from the donor bone marrow. Both CD4 and CD8 cells are involved in this process, but CD4 cells are required to activate CD8+ T cells. Eliminating recipient's CD4+ T cells would therefore allow successful grafting. Removal of CD4+ T cells specific for alloantigens require a high performance affinity adsorption because of the low frequency of such cells.

[0162]The prior art MHC —T cell epitope complexes have not the required affinity to detect and to isolate the relevant CD4+ cells.

[0163]In the mouse model, male bone marrow is rejected by syngeneic females due to recognition of H-Y encoded antigens among which the Dby protein plays a major role. A majority of CD4+ T cells recognize an epitope made of residues FNSNRANSS of the murine Dby antigen which is encoded by the H-Y chromo...

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PUM

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Abstract

The present invention relates an in vitro method for detecting class II restricted CD4+ T cells in a sample. Herein a sample is contacted with an isolated complex of an MHC class II molecule and a peptide. This peptide comprises an MHC class II restricted T cell epitope of an antigenic protein and immediately adjacent thereof, or separated by a linker of at most 7 amino acids a sequence with a [CST]-xx-C or C-xx-[CST] motif. CD4+ T cells are detected by measuring the binding of the complex with cells in the sample, wherein the binding of the complex to a cell is indicative for the presence of CD4+ T cells in the sample. The present invention further relates to an isolated complex of an MHC Class II molecule and a peptide comprising an MHC class II restricted T cell epitope of an antigenic protein and immediately adjacent thereof, or separated by a linker of at most 7 amino acids a sequence with a [CST]-xx-C or C-xx-[CST] motif.

Description

FIELD OF INVENTION[0001]The present invention relates to synthetic peptides encompassing class I l-restricted major histocompatibility complex (MHC) T cell epitopes containing a thioredox motif within flanking residues for the detection, preparation or depletion of CD4+ T lymphocytes in or from body fluids or culture medium.BACKGROUND OF THE INVENTION[0002]Lymphocytes play a central role in the elaboration of immune responses against foreign antigens and in the control of diseases. Such recruitment and activation of lymphocytes can be beneficial as in responses against infectious agents, or detrimental, such as exemplified by auto-immune diseases, responses to allergens and in graft rejection. There are therefore a large number of circumstances in which it would be advantageous to detect, enumerate, purify or deplete such lymphocytes. Current methods to achieve these goals are, however, unsatisfactory.[0003]Lymphocytes are divided in several lineages and subsets according to the pre...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): G01N33/569C07K14/725C07K14/74C07K17/14
CPCG01N33/56972C07K14/70539C07K17/14C07K2319/00G01N2333/70539G01N2333/70514G01N2469/10C07K14/7051G01N33/505A61K2039/605A61P43/00C07K14/70514G01N33/56977
Inventor SAINT-REMY, JEAN-MARIECARLIER, VINCENTVANDER, ELST, LUC
Owner IMCYSE
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