Immune modulation via C-type lectin
An immune response and antigen technology, applied in immunoglobulin, anti-animal/human immunoglobulin, allergic diseases, etc., can solve problems such as unknown binding specificity correlation
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2010-11-24
- Estimated Expiration
- Not applicable · inactive patent
Smart Images
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Abstract
Description
technical field
[0001] The present invention relates to the regulation of the immune system, in particular the use of molecules with affinity for CLEC9a molecules to elicit and suppress immune responses against target antigens. Background technique
[0002] The immune system is able to detect the presence of infectious agents and mount a response against them without destroying its own tissues. This phenomenon is unusual due to the great molecular diversity of pathogens and their high replication and mutation rates. Multicellular organisms have been motivated to develop a variety of different immune recognition systems during the evolution process, namely "innate" and "adaptive" immune systems.
[0003] The evolutionarily ancient innate immune system detects the presence and nature of infection, provides the first line of host defense, and controls the initiation and determination of the adaptive immune system's effector classes.
[0004] Dendritic cells (DCs) play a pivot...
Examples
Embodiment
[0245] Sequence and structure of CLEC9a
[0246] A search of the NCBI gene database revealed that CLEC9a sequences have been identified in mice (Mus musculus), apes (Pan troglodytes), humans (Homo sapiens) and rhesus monkeys (Macaca mulatta). A blast search using the mouse CLEC9a protein sequence also revealed predicted CLEC9a proteins in rat (Rattus norvegicus), dog (Canis familiaris) and bovine (Bostaurus). The human cDNA sequence and its representative protein sequence with related domains are in figure 1 described in detail. The mouse cDNA sequence and its representative protein sequence that we cloned from mouse CD8α+DC are in figure 2 in detail. This sequence differs from the published cDNA sequence in that it contains an additional G residue, causing a frameshift to the end of the molecule, resulting in a relatively figure 2 Longer proteins shown in . Our sequence appears to be correct as it matches the published genome sequence (NC_000072.4GI:94471533); as seen ...