Abstract 1035P
Background
To investigate new mechanisms for regulation of pathological IL-6 production.
Methods
Interleukin-6 synthesis was studied in PBMC cultures, either spontaneous in autologous cultures or stimulated by serum factors or specific peptides. Immunoregulatory albumin neo-structures were identified using 2D-gel electrophoresis and MALDI-TOF-MS. The neo-structures in serum or culture supernatants were determined by ELISA.
Results
PBMC in autologous cultures from cancer patients produce large amounts of IL-6, even in early-stage disease. Proteolytic degradation of albumin generates an IL-6 inducing neo-structure, P935, found in tumours, serum and urine. This neo-structure is immunogenic and elicits autoantibodies, resulting in immune complexes. The free neo-structure, identified by “Artificial Cell Surface Chromatography”, induces IL-6 by healthy PBMC. Such IL-6 production is inhibited by specific rabbit antibodies or by specific autoantibodies. The serum concentration of this IL-6 inducing factor, IL-6IF, is significantly higher in advanced cancer stages and is significantly correlated to the over-all survival of the patients.
Conclusions
A new mechanism for induction of IL-6 synthesis is presented. Based on this mechanism the pathological IL-6 production related to an enhanced proteolytic activity can be diagnosed and selectively inhibited by specific antibodies. Thus, the neo-structures, inducing pathological IL-6 production, associated with a reduced survival of cancer patients can be selectively removed by therapeutic administration of specific antibodies, leaving the function of IL-6 needed for the normal activity of the immune system intact.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Swedish State under the LUA/ALF agreement (ALFGBG-966007) and the Swedish Cancer Society (CAN 22 2370). Health Research Council in the South East of Sweden. Canimguide Therapeutics AB, Therim Diagnostica AB, Sweden.
Disclosure
L. Håkansson: Other, Personal, Ownership Interest: Therim Diagnostica AB. A. Hakansson: Financial Interests, Personal, Stocks/Shares: Therim Diagnostica AB. All other authors have declared no conflicts of interest.
Resources from the same session
1003P - A first-in-human (FIH) phase I study of IPH5301, an anti-CD73 monoclonal antibody (mAb), in patients with advanced solid tumors (AST) (CHANCES, NCT05143970)
Presenter: Mathilde Beaufils
Session: Poster session 03
1004P - Phase I/II trial of ASP1570, a novel diacylglycerol kinase ζ inhibitor, in patients with advanced solid tumors
Presenter: Daniel Olson
Session: Poster session 03
1005P - Microbial ecosystem therapeutics 4 (MET4) treatment mediates a humoral response in patients treated with immune checkpoint inhibition (ICI)
Presenter: Pavlina Spiliopoulou
Session: Poster session 03
1007P - Systemic STING agonist BI 1703880 plus ezabenlimab in patients (pts) with advanced solid tumors: Initial results from a phase Ia study
Presenter: Kevin Harrington
Session: Poster session 03
1008P - Preliminary clinical PK and PD analysis of a phase I study of ZL-1218, a humanized anti-CCR8 IgG1 antibody, in patients with advanced solid tumors
Presenter: Ignacio Gil Bazo
Session: Poster session 03
1010P - Phase I dose-escalation study of HBM1020: A novel anti-B7H7 antibody in patients with advanced solid tumors
Presenter: Jason Henry
Session: Poster session 03
1011P - Model-informed dose optimization of HFB200301, a TNFR2 agonist monoclonal antibody (mAb), in monotherapy and in combination with the anti-PD-1 mAb tislelizumab (TIS), in patients (pts) with advanced solid tumors
Presenter: Desamparados Roda Perez
Session: Poster session 03
1012P - Safety, tolerability, and efficacy of nadunolimab in combination with pembrolizumab in patients with solid tumors
Presenter: roger cohen
Session: Poster session 03
1013P - A phase I study of rivoceranib combined with nivolumab in patients with unresectable or metastatic cancer
Presenter: Neal Chawla
Session: Poster session 03