Feng et al., 2025 - Google Patents
Common connective tissue disorder and anti-cytokine autoantibodies are enriched in idiopathic multicentric castleman disease patientsFeng et al., 2025
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- 17773630647223233351
- Author
- Feng A
- Gonzalez M
- Kalaycioglu M
- Yin X
- Mumau M
- Shyamsundar S
- Bustamante M
- Chang S
- Dhingra S
- Dodig-Crnkovic T
- Schwenk J
- Garg T
- Yoshizaki K
- van Rhee F
- Fajgenbaum D
- Utz P
- Publication year
- Publication venue
- Frontiers in Immunology
External Links
Snippet
Introduction Idiopathic Multicentric Castleman Disease (iMCD) is a polyclonal lymphoproliferative disorder involving cytokine storms that can lead to organ failure and death. The cause of iMCD is unknown, but some clinical evidence suggests an autoimmune …
- 208000032641 idiopathic multicentric Castleman disease 0 title abstract description 22
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- G01N33/53—Immunoassay; Biospecific binding assay
- G01N33/564—Immunoassay; Biospecific binding assay for pre-existing immune complex or autoimmune disease, i.e. systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, rheumatoid factors or complement components C1-C9
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- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6863—Cytokines, i.e. immune system proteins modifying a biological response such as cell growth proliferation or differentiation, e.g. TNF, CNF, GM-CSF, lymphotoxin, MIF or their receptors
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- G01N2333/52—Assays involving cytokines
- G01N2333/521—Chemokines
- G01N2333/523—Beta-chemokines, e.g. RANTES, I-309/TCA-3, MIP-1alpha, MIP-1beta/ACT-2/LD78/SCIF, MCP-1/MCAF, MCP-2, MCP-3, LDCF-1or LDCF-2
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