scholarly journals A screening strategy to identify novel immunomodulators

2021 ◽  
Author(s):  
◽  
Vimal Patel

<p>Understanding the immunomodulatory activities of compounds is important to identify the unintended adverse immunomodulatory effects of therapeutic compounds in development and to select novel compounds that may provide benefit for those diagnosed with immunemediated disorders. In both these cases, it is desirable to identify compounds with immunomodulatory activity early in the drug discovery process in a medium-throughput format. A screening strategy has been designed to fulfil these needs.  The first step in designing the strategy was to select informative assays and optimise individual assays to suit medium-throughput drug discovery. These individual assays investigated effects on a broad range of functions associated with innate and adaptive immune cells including macrophages (activation, cytokine production, phagocytosis and motility), helper T cells (activation and cytokine production), cytotoxic T cells (degranulation and cytokine production), and B cells (antibody production and cytokine production). Cost effectiveness and ease-of-use were important considerations during assay design and optimisation.  Using a compound set comprised of positive controls (i.e. compounds known to alter specific immune functions), a data set was generated to guide the strategy design. Assays were ordered to efficiently use resources and reduce the generation of less informative data. Additionally, using data collected from this compound set, strategies to assess and identify immunomodulatory activity were built and analysed. A second set of compounds was used to validate the screening strategy, and this screen highlighted new and novel activities for these known compounds that suggests they possess additional immunomodulatory effects.  Once validated, several novel compounds were run through the screen, including a traditional Samoan medicine, a heparan sulfate mimetic, and a novel anti-cancer agent; unique immunomodulatory activities were discovered. Finally, a hierarchical cluster analysis was used to cluster compounds sharing similar activity profiles and suggested the potential to develop further statistical methods to provide insight into compound characterisation. Together, this research has developed and validated a novel, medium throughput drug discovery system that can facilitate the identification of the immunomodulatory activities of compounds in the drug discovery environment.</p>

2021 ◽  
Author(s):  
◽  
Vimal Patel

<p>Understanding the immunomodulatory activities of compounds is important to identify the unintended adverse immunomodulatory effects of therapeutic compounds in development and to select novel compounds that may provide benefit for those diagnosed with immunemediated disorders. In both these cases, it is desirable to identify compounds with immunomodulatory activity early in the drug discovery process in a medium-throughput format. A screening strategy has been designed to fulfil these needs.  The first step in designing the strategy was to select informative assays and optimise individual assays to suit medium-throughput drug discovery. These individual assays investigated effects on a broad range of functions associated with innate and adaptive immune cells including macrophages (activation, cytokine production, phagocytosis and motility), helper T cells (activation and cytokine production), cytotoxic T cells (degranulation and cytokine production), and B cells (antibody production and cytokine production). Cost effectiveness and ease-of-use were important considerations during assay design and optimisation.  Using a compound set comprised of positive controls (i.e. compounds known to alter specific immune functions), a data set was generated to guide the strategy design. Assays were ordered to efficiently use resources and reduce the generation of less informative data. Additionally, using data collected from this compound set, strategies to assess and identify immunomodulatory activity were built and analysed. A second set of compounds was used to validate the screening strategy, and this screen highlighted new and novel activities for these known compounds that suggests they possess additional immunomodulatory effects.  Once validated, several novel compounds were run through the screen, including a traditional Samoan medicine, a heparan sulfate mimetic, and a novel anti-cancer agent; unique immunomodulatory activities were discovered. Finally, a hierarchical cluster analysis was used to cluster compounds sharing similar activity profiles and suggested the potential to develop further statistical methods to provide insight into compound characterisation. Together, this research has developed and validated a novel, medium throughput drug discovery system that can facilitate the identification of the immunomodulatory activities of compounds in the drug discovery environment.</p>


1992 ◽  
Vol 20 (03n04) ◽  
pp. 233-243 ◽  
Author(s):  
Yee-Shin Lin ◽  
Hsuch-Ching Chiang ◽  
Woei-Song Kan ◽  
Emily Hone ◽  
Shyh-Jen Shih ◽  
...  

The immunomodulatory effects of Physalis angulata L. extract fraction VII (PA-VII), PA-VII-A, PA-VII-B and PA-VII-C were investigated in this study. The results showed that PA-VII and PA-VII-C strongly enhanced blastogenesis response, PA-VII-B had moderate activity, and PA-VII-A exerted only slight effect on cell proliferation. A synergistic effect was observed when the suboptimal dosage of phytohemagglutinin (PHA) or lipopolysaccharide (LPS) was added to the culture. Furthermore, PA-VII and PA-VII-C possessed stimulatory activity on B cells and less effect on T cells. The antibody responses were also augmented by PA-VII, PA-VII-B and PA-VII-C, but not by PA-VII-A. The enhancement of antibody response could be observed both in BALB/c and C3H/HeJ mice.


2017 ◽  
Vol 5 (1) ◽  
pp. e417 ◽  
Author(s):  
Ann Ranger ◽  
Soma Ray ◽  
Suzanne Szak ◽  
Andrea Dearth ◽  
Norm Allaire ◽  
...  

Objective:To evaluate whether the anti-LINGO-1 antibody has immunomodulatory effects.Methods:Human peripheral blood mononuclear cells (hPBMCs), rat splenocytes, and rat CD4+ T cells were assessed to determine whether LINGO-1 was expressed and was inducible. Anti-LINGO-1 Li81 (0.1–30 μg/mL) effect on proliferation/cytokine production was assessed in purified rat CD4+ T cells and hPBMCs stimulated with antibodies to CD3 +/– CD28. In humans, the effect of 2 opicinumab (anti-LINGO-1/BIIB033; 30, 60, and 100 mg/kg) or placebo IV administrations was evaluated in RNA from blood and CSF samples taken before and after administration in phase 1 clinical trials; paired samples were assessed for differentially expressed genes by microarray. RNA from human CSF cell pellets was analyzed by quantitative real-time PCR for changes in transcripts representative of cell types, activation markers, and soluble proteins of the adaptive/innate immune systems. ELISA quantitated the levels of CXCL13 protein in human CSF supernatants.Results:LINGO-1 is not expressed in hPBMCs, rat splenocytes, or rat CD4+ T cells; LINGO-1 blockade with Li81 did not affect T-cell proliferation or cytokine production from purified rat CD4+ T cells or hPBMCs. LINGO-1 blockade with opicinumab resulted in neither significant changes in immune system gene expression in blood and CSF, nor changes in CXCL13 CSF protein levels (clinical studies).Conclusions:These data support the hypothesis that LINGO-1 blockade does not affect immune function.Classification of evidence:This study provides Class II evidence that in patients with MS, opicinumab does not have immunomodulatory effects detected by changes in immune gene transcript expression.


2015 ◽  
Vol 1 (2) ◽  
pp. 122-128
Author(s):  
Syuichi Koarada ◽  
Yuri Sadanaga ◽  
Natsumi Nagao ◽  
Satoko Tashiro ◽  
Rie Suematsu ◽  
...  

2019 ◽  
Vol 8 (2) ◽  
pp. 227-237 ◽  
Author(s):  
Alexandra E. Turley ◽  
Joseph W. Zagorski ◽  
Rebekah C. Kennedy ◽  
Robert A. Freeborn ◽  
Jenna K. Bursley ◽  
...  

The purpose of this study was to determine the effect of subchronic, oral, low-dose cadmium exposure (32 ppm over 10 weeks) on the rat immune system. We found that cadmium exposure increased the induction of IFNγ and IL-10 in T cells activated ex vivo after cadmium exposure.


Blood ◽  
2003 ◽  
Vol 101 (11) ◽  
pp. 4253-4259 ◽  
Author(s):  
Elodie Belnoue ◽  
Michèle Kayibanda ◽  
Jean-Christophe Deschemin ◽  
Mireille Viguier ◽  
Matthias Mack ◽  
...  

Abstract Infection of susceptible mouse strains with Plasmodium berghei ANKA (PbA) is a valuable experimental model of cerebral malaria (CM). Two major pathologic features of CM are the intravascular sequestration of infected erythrocytes and leukocytes inside brain microvessels. We have recently shown that only the CD8+ T-cell subset of these brain-sequestered leukocytes is critical for progression to CM. Chemokine receptor–5 (CCR5) is an important regulator of leukocyte trafficking in the brain in response to fungal and viral infection. Therefore, we investigated whether CCR5 plays a role in the pathogenesis of experimental CM. Approximately 70% to 85% of wild-type and CCR5+/- mice infected with PbA developed CM, whereas only about 20% of PbA-infected CCR5-deficient mice exhibited the characteristic neurologic signs of CM. The brains of wild-type mice with CM showed significant increases in CCR5+ leukocytes, particularly CCR5+ CD8+ T cells, as well as increases in T-helper 1 (Th1) cytokine production. The few PbA-infected CCR5-deficient mice that developed CM exhibited a similar increase in CD8+ T cells. Significant leukocyte accumulation in the brain and Th1 cytokine production did not occur in PbA-infected CCR5-deficient mice that did not develop CM. Moreover, experiments using bone marrow (BM)–chimeric mice showed that a reduced but significant proportion of deficient mice grafted with CCR5+ BM develop CM, indicating that CCR5 expression on a radiation-resistant brain cell population is necessary for CM to occur. Taken together, these results suggest that CCR5 is an important factor in the development of experimental CM.


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