Methods of modulating hvem, btla and cd160 cis complex response or signaling activity with soluble light polypeptide sequences

a cis complex and soluble light polypeptide technology, applied in the field of hvem cis complexes, can solve the problems of unsafe application and poorly understood cosignaling pathway, and achieve the effects of inhibiting or preventing spontaneous multimerization of hvem, preventing recruitment, and inhibiting trans activation of hvem

Inactive Publication Date: 2010-05-27
LA JOLLA INST FOR ALLERGY & IMMUNOLOGY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Benefits of technology

[0009]As disclosed herein, BTLA and HVEM form a “cis” complex, and CD160 and HVEM form a “cis” complex. HVEM cis complex formation with BTLA limits the activation HVEM by its cellular ligands. Naïve T cells (e.g., human and mouse) express a stable heterodimeric “cis” complex of HVEM and BTLA that uses the same binding interaction as the trans complex. This HVEM-BTLA “cis” complex competitively inhibits trans signaling by all cellular ligands of HVEM, which can provide, among other things, a mechanism to maintain T cells in a resting state. Thus, the context of HVEM expression (cis or trans) with its various ligands determines signaling outcome: bidirectional signaling of HVEM in a trans complex can provide survival signaling for activated T cells, and HVEM in cis interactions in naïve T cells limits receptivity to signals from cells, such as those in the surrounding microenvironment.
[0010]As also disclosed herein, the conformation of HVEM in cis or t

Problems solved by technology

The mechanisms of action of some of these cosignaling pathways are poorly understood and have resulted in unsafe application such as in the case of CD28 targeted therapy (S

Method used

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  • Methods of modulating hvem, btla and cd160 cis complex response or signaling activity with soluble light polypeptide sequences
  • Methods of modulating hvem, btla and cd160 cis complex response or signaling activity with soluble light polypeptide sequences
  • Methods of modulating hvem, btla and cd160 cis complex response or signaling activity with soluble light polypeptide sequences

Examples

Experimental program
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example 1

This Example Describes Materials and Methods Used in Examples 2 to 12

Reagents and Cell Lines

[0153]Antibodies used included: mouse anti-BTLA mAb (J168, IgG1κ; BD Bioscience, San Diego, Calif.), mouse anti-HVEM mAb (clone 94801, R&D System, Emeryville, Calif.), mouse anti-mouse BTLA mAb (6F7), Armenian Hamster anti-HVEM mAb (LH1), mouse anti-human HVEM (eBioHVEM-122), and mouse anti-human BTLA (MIH26) (eBioscience, San Diego, Calif.); mouse anti-FLAG mAb (M2 clone, Sigma-Aldrich, St. Louis, Mo.), rabbit-anti-RelA / p65 Ab (C-20), anti-RelB (C-19) and anti-TRAF3 Ab (H-122) (Santa Cruz Biotechnology) and rat anti-TRAF2 mAb (6F8 clone, MBL, Nagoya, Japan). Rat anti-BTLA mAb (6F4, IgG1κ), goat anti-HVEM and anti-LTβR IgG were made in-house against purified receptor Fc proteins as described (Rooney, et al., Methods Enzymol 322:345 (2000)). Purified Fc fusion proteins: HVEM-Fc, BTLA-Fc and LTβR-Fc, of mouse or human origin, were produced and purified as described (Cheung, et al., Proc Natl Ac...

example 2

This Example Includes Studies Showing Expression Patterns of Intrinsic BTLA and HVEM Complex in T cells

[0164]The possibility that HVEM and BTLA act in cis, implicated T cells may coexpress HVEM and BTLA. The expression patterns of HVEM and BTLA in mouse and human naïve T cells isolated from spleen or peripheral blood, respectively using specific mAb were studied. Indeed, the vast majority of CD3+T cells obtained from human and mouse coexpressed HVEM and BTLA, suggesting a pattern of expression conserved across species. Both major subsets of mouse T lymphocytes coexpressed HVEM and BTLA with CD4 T cells expressing relatively more BTLA than CD8 T cells.

example 3

This Example Includes Studies Showing Cis-Interaction Between HVEM and BTLA

[0165]Dendritic cells, and T and B lymphocytes depending on their state of activation, coexpress HVEM and BTLA (De Trez, et al., J Immunol (2008) 180:238; Sedy, et al., Nat Rev Immunol (2005) 8:861) indicating the potential for ligand receptor complex formation in cis. To determine whether HVEM and BTLA form a complex when coexpressed in the same cells, 293T cells were transfected with BTLA, HVEM or both, and HVEM immunoprecipitated from lysates with aid of a Flag-epitope tag (HVEM-Flag). BTLA specifically coimmunoprecipitated with HVEM-Flag in cells coexpressing HVEM and BTLA (FIG. 1A, lane 4). In contrast, BTLA did not associate with HVEM when immunoprecipitated from a mixture of HVEM expressing 293T cells (293T-HVEM) and BTLA expressing 293T cells (293T-BTLA) (FIG. 1A, lane 3). This result indicated HVEM-BTLA forms a stable complex in cis, but not in trans.

[0166]To measure HVEM and BTLA interactions in nat...

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Abstract

The invention provides HVEM cis complexes which include, for example, HVEM/BTLA, HVEM/CD160 and HVEM/gD cis complexes. The invention provides ligands and agents that bind to HVEM cis complexes, such as antibodies. The invention further provides methods of use of the HVEM cis complexes, and the ligands and agents (e.g., LIGHT polypeptide sequence) that bind to the HVEM cis complexes.

Description

RELATED APPLICATIONS[0001]This application is a continuation-in-part and claims the benefit of priority of PCT international application no. PCT / US2009 / 49968, filed Jul. 8, 2009, application Ser. No. 61 / 078,997, filed Jul. 8, 2008, application Ser. No. 11 / 721,308, filed Jun. 8, 2007, PCT international application no. PCT / US2005 / 044296, filed Dec. 9, 2005, application Ser. No. 60 / 770,636, filed Jul. 19, 2005, and application Ser. No. 60 / 635,034, filed Dec. 9, 2004, all of which applications are expressly incorporated herein by reference in their entirety.GOVERNMENT SUPPORT[0002]This work was supported in part by Grants R37AI33068 and AI067890 from the National Institutes of Health. The government has certain rights in the invention.TECHNICAL FIELD[0003]The invention relates to HVEM cis complexes. Such HVEM cis complexes include, for example, HVEM / BTLA, HVEM / CD160 and HVEM / gD cis complexes. Furthermore, the invention relates to ligands and agents that bind to HVEM cis complexes, such ...

Claims

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Application Information

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IPC IPC(8): A61K39/00A61P37/06
CPCC07K16/2803C07K16/2818C07K16/2878A61K39/0005C07K2319/30G01N2333/70578C07K2316/96C07K2317/73C07K2317/74C07K2317/75C07K2317/76A61P25/28A61P29/00A61P35/00A61P37/02A61P37/06
Inventor WARE, CARL F.CHEUNG, TIMOTHY C.STEINBERG, MARCOS
Owner LA JOLLA INST FOR ALLERGY & IMMUNOLOGY
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