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  2. CD38 - Wikipedia

    en.wikipedia.org/wiki/CD38

    CD38 (cluster of differentiation 38), also known as cyclic ADP ribose hydrolase, is a glycoprotein ... which becomes the major cause of NAD+ depletion with age.

  3. Daratumumab - Wikipedia

    en.wikipedia.org/wiki/Daratumumab

    Daratumumab binds to a different CD38 epitope amino-acid sequence than does the anti-CD38 monoclonal antibody isatuximab. [21] Daratumumab binds to CD38, causing cells to apoptose via antibody-dependent cellular cytotoxicity , complement-dependent cytotoxicity , inhibition of mitochondrial transfer or antibody-dependent cellular phagocytosis .

  4. Isatuximab - Wikipedia

    en.wikipedia.org/wiki/Isatuximab

    Isatuximab, sold under the brand name Sarclisa, is a monoclonal antibody (mAb) medication for the treatment of multiple myeloma. [6] [4]The most common side effects include neutropenia (low levels of neutrophils, a type of white blood cell), infusion reactions, pneumonia (infection of the lungs), upper respiratory tract infection (such as nose and throat infections), diarrhoea and bronchitis ...

  5. Plasma cell - Wikipedia

    en.wikipedia.org/wiki/Plasma_cell

    Human LLPC population can be identified as CD19 – CD38 hi CD138 + cells. [17] The long-term survival of LLPC are dependent on a specific environment in the bone marrow, the plasma cell survival niche. [18] Removal of an LLPC from its survival niche results in its rapid death.

  6. Myeloid-derived suppressor cell - Wikipedia

    en.wikipedia.org/wiki/Myeloid-derived_suppressor...

    MDSC depletion restored the function of impaired hepatic NK cells. An MDSC derived from chronic inflammation caused T and NK-cell dysfunction along with downregulation of the TCR z chain (CD247). The immunosuppressive milieu directly affects CD247, which is crucial in initiating immune responses.

  7. CD19 - Wikipedia

    en.wikipedia.org/wiki/CD19

    CD19 is widely expressed during all phases of B cell development until terminal differentiation into plasma cells. During B cell lymphopoiesis, CD19 surface expression starts during immunoglobulin (Ig) gene rearrangement, which coincides during B lineage commitment from hematopoietic stem cell. [8]