Lymphomas represent a set of lymphoid cell malignancies that can range from indolent to aggressive. B cell-derived lymphomas, specifically non-Hodgkin lymphoma (NHL), are the most prevalent, but this disease can also originate from T cells. In 2018, an estimated 74,680 new cases of NHL in the United States will be diagnosed, and 19,910 patient deaths will occur. While the five-year survival rate for NHL is relatively high at 71%, recurrence is common, so continued discovery of improved treatments for lymphoma is important for long term survival of these patients.
Researchers use preclinical mouse modeling of lymphoma to explore novel combination strategies of conventional chemotherapy or radiation and immunomodulatory agents. To support these efforts, MI Bioresearch has developed the murine B cell lymphoma model, A20. A20 was derived from a spontaneous reticulum cell sarcoma from an aging Balb/c mouse. A20 tumors are reported to express PD-L1, which is consistent with our RNAseq profile (data not shown) and concordant with several human lymphoma subtypes, making it attractive for use in immunotherapy drug development.
In a 2017 Model Spotlight, we presented initial growth data as well as response to therapy initiated soon after a subcutaneous implant. In 2018, we continued efforts to expand characterization of this model. Herein we present initial anti-tumor response data in established subcutaneous A20 tumors as well as present growth kinetics of a systemic luciferase-enabled A20 model with tumor progression monitored by bioluminescence imaging (BLI).
Treatment of A20 with immunotherapy agents in vivo is extremely effective against early stage disease, resulting in several complete responses. However, as expected, initiating treatment once tumors are established results in a much more limited response. Figure 1 illustrates individual (A-F) growth of control tumors and those treated with anti-mPD-1 or anti-mPD-L1 as monotherapy or in combination with focal radiation delivered by SARRP (XStrahl). Combination therapy produced a better than additive anti-tumor response, indicating that these strategies can be readily assessed in the A20 model once the tumors are established. Additionally, efficacy of anti-mGITR and anti-mCD137 against established A20 tumors was minimal to moderate, allowing for a broad dynamic range to assess improvement in combination of these antibodies and investigational agents (Figure 2 A-C).
To further increase utility of the A20 lymphoma model, we luciferase-enabled the A20 cell line which can be used to monitor tumor progression of systemic disease. The median doubling time of the model is 2.7 days with a therapeutic window of approximately three weeks.
Figure 3 shows individual tumor progression determined by BLI (A) and overall survival (B) which indicates favorable growth kinetics, and Figure 4 illustrates representative BLI imaging over time. Upon necropsy, a 100% incidence of liver lesions and 70% incidence of hindlimb paralysis and/or lesions on other organs (i.e., spleen, ovary, pancreas) were recorded. Abdominal distension was a common clinical sign manifesting between Days 30-32 and correlates well to the timing of strong BLI signal in Figures 3 and 4. A follow up study to investigate response to checkpoint blockade and costimulatory molecules is ongoing using this systemic model.
The A20 model provides robust preclinical means by which to study B cell lymphoma both by subcutaneous and systemic methods. Please contact MI Bioresearch to speak with our scientists about how A20 or one of our other syngeneic models can be used for your next immuno-oncology study.
 Howlader N, Noone AM, Krapcho M, Miller D, Bishop K, Kosary CL, Yu M, Ruhl J, Tatalovich Z, Mariotto A, Lewis DR, Chen HS, Feuer EJ, Cronin KA (eds). SEER Cancer Statistics Review, 1975-2014, National Cancer Institute. Bethesda, MD, https://seer.cancer.gov/csr/1975_2014/, based on November 2016 SEER data submission, posted to the SEER web site, April 2017.
 Kim KJ, Kanellopoulos Langevin C, Merwin RM, Sachs DH, Asofsky R (1979) Establishment and characterization of BALB/c lymphoma lines with B cell properties. Journal of Immunology, 122(2): 549–554.
 Sagiv-Barfi I, Kohrt HEK, Czerwinski DK, Ng PP, Chang BY, Levy L (2015) Therapeutic antitumor immunity by checkpoint blockade is enhanced by ibrutinib, an inhibitor of both BTK and ITK. PNAS, 112(9): E966-E972.
 Gatalica Z, Bilalovic N, Vranic S, Arguello D, Reddy S, and Ghosh N (2015) PD-L1 and PD1 Expression in Lymphomas. Blood, 126; 3899.
About the Author: Sheri Barnes joined MI Bioresearch in 2017 as Director, Scientific Development. Prior to joining MI Bioresearch, she served as a Study Director at Charles River Laboratories. She has fourteen years of experience in the CRO industry, with the past eleven years focused on using in vivo oncology research models in drug development. Sheri holds a Ph.D. in Cell and Developmental Biology from University of North Carolina at Chapel Hill.