1 / 32

Skin Sensitization and AOP

Skin Sensitization and AOP. Quanshun Zhang and Erin Hill Institute for In Vitro Sciences, Inc. 30 West Watkins Mill Road Gaithersburg, Maryland 20878 USA www.iivs.org. Mechanism of Skin Sensitization.

roosa
Télécharger la présentation

Skin Sensitization and AOP

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Skin Sensitization and AOP Quanshun Zhang and Erin Hill Institute for In Vitro Sciences, Inc. 30 West Watkins Mill Road Gaithersburg, Maryland 20878 USA www.iivs.org

  2. Mechanism of Skin Sensitization Subsequent skin contact with chemical activates the T cells and leads to clinical manifestation LLNA Chemical (hapten) penetrates skin and reacts with protein(s) INDUCTION ELICITATION Inflammation EPIDERMIS DERMIS Chemical is recognized by Langerhans cells which then migrate from the skin to the draining lymph node Increased number of chemical-specific T-cells released into the systemic circulation This causes proliferation of specific T cells Lymph node Mature LC presents chemical to T cells D. Basketter

  3. Clinical Manifestation

  4. Skin Sensitization Endpoint Evolution(animal based methods) Mouse Local Lymph Node Assay (LLNA) OECD TG 429 (2010) Human repeat insult patch testing (HRIPT) Guinea Pig Test Methods OECD TG 406 (1992)

  5. Local Lymph Node Assay (LLNA) Days 1, 2, 3 apply chemical to ear • Identifies skin sensitizing chemicals as a function of their ability to provoke T lymphocytes proliferative response in draining lymph nodes • LLNA reduced and refined animal use • Practical considerations: less time (7 days), cheaper, quantitative endpoint, potency information • LLNA has been validated as a replacement of the older guinea pig tests Days 6 – inject 3H thymidine 5 h- Remove lymph nodes, quantify incorporated 3H

  6. HRIPT (Human Repeat Insult Patch Testing) • Used for decades for diagnosis of skin allergy • A small patch of test article is applied/reapplied • After rest period, the test material is applied again • Contact allergy: redness, swelling, itchiness • Ethical concerns for testing in volunteers: may elicit clinical disease in the volunteers

  7. Skin Sensitization Endpoint Evolution(alternatives to animal based methods) In Silico Methods Times-SS DEREK OECD Toolbox In Chemico Reactivity Assays DPRA (OECD TG 442C) In Vitro Cell Based Assays ARE-Reporter Assays h-Clat (OECD 442D & 442E)

  8. Toolbox of Non-Animal Methods Adapted; Natch and Emter. Arch Toxicol2015 ,(89) 1645-1668

  9. AOP Tools for Skin Sensitization Molecular properties Organism Response Cellular Response Molecular Initiating Event Organ Response KeratinoSens (TG 442D) LuSens(TG 442D, pending) SENS-IS (Under validation) h-CLAT (TG 442E) U-SENS (TG442E) IL-8-Luc Assay (TG442E) GARD (Under review) AREc32 EE Potency assay mMUSST/MUSST DPRA(TG 442C) PPRA kDPRA In Silico, QSAR Human T Cell Proliferation Assay HRIPT Buehler (TG 406) LLNA (TG 429 and 442 A/B)

  10. Key Event 1- Haptenation:Direct Peptide Reactivity Assay (DPRA) • Addresses haptenation (MIE) Key Event 1 • Developed by Gerberick and colleagues at P&G • A skin sensitizer forms covalent bonds with peptides • Test Article – Peptide mixture incubation of 24 hours • Cysteine & lysine peptide depletion monitored by HPLC Nucleophilic-electrophilic interaction: Chemical Allergen :Nu Chemical allergen E Protein Cysteine, Lysine Protein

  11. DPRA HPLC Un-reacted Peptide Chemical Allergen Protein Chemical Allergen Test Chemical Peak Area of un-reacted peptide is compared to peak area of reacted peptide Reaction Mixture Protein

  12. DPRA Example Data Set Cinnamic Aldehyde Glycerol %Depletion = 0% %Depletion = 77.5%

  13. Key Event 2- Activation of ARE Pathway: KeratinoSens Assay • Addresses keratinocyte responses by activation of antioxidant/electrophile response element dependent pathway (Keap1-Nrf2-ARE) Key event 2 • sensitizers are electrophilic, or potential to be transformed to electrophilic chemicals • The Nrf-2-electrophile sensing pathway comprising the repressor protein Keap1, the transcription factor Nrf2 and the antioxidant response element (ARE) detects skin sensitizers H S H S Nrf2 Luciferase Keap I ARE-element Nrf2

  14. KeratinoSens Data Analysis • Gene induction compared to DMSO control wells • EC1.5 = concentration for induction above 1.5 threshold • Positive Response: • EC1.5 value below 1000 µM in at least 2 of 3 repetitions • At the lowest concentration with induction >1.5, viability >70% • Apparent overall dose response, similar between repetitions Non-Sensitizer Sensitizer

  15. T T T T Key Event 3- Expression of Adhesion/ Co-Stimulatory Molecules Induction phase • Langerhans cells (LC) play a critical role in skin sensitization • Upon antigen capture, LC undergo maturation and migrate to the draining lymph nodes • LC maturation is characterized by the up-regulation of CD86 and CD54 (Aiba and Katz, 1990; Ozawa et al., 1996) allergens LC activation T-cell proliferation Lymph node Image from Jowsey et al.

  16. Human Cell Line Activation Test (h-CLAT) • Addresses Dendritic Cell (DC) responses by measuring expression of co-stimulatory and adhesion molecules using THP-1 cells: Key event 3 • RFI CD86 ≥150% and CD54 ≥200%with cell viability of ≥50% in at least 2 independent repetitions relative to vehicle controls

  17. Integrated Testing Strategies (ITS) OECD Test Guidelines for 3 methods (others under review) • Direct Peptide Reactivity Assay (DPRA) (TG 442C) (2015) • ARE-Nrf2 Luciferase Method (KeratinoSensTM) (TG 442D) (2015) • Human Cell Line Activation Test (h-CLAT) (TG 442E) (2016) • OECD- support discrimination between skin sensitizers (UN GHS category 1) and non-sensitizers in combination with other info • Each assay considered for an Integrated Testing Strategy (ITS) for hazard identification; development of Adverse Outcome Pathway (AOP) • Individual assay limitations, integrated approach better • For safety determination, all 3 assays should be used • Test Guidelines cannot be used on their own to sub-categorize skin sensitizers into UN GHS subcategories 1A and 1B or to predict potency for safety assessment identification

  18. Mechanism of Skin Sensitization Subsequent skin contact with chemical activates the T cells and leads to clinical manifestation LLNA Chemical (hapten) penetrates skin and reacts with protein(s) INDUCTION ELICITATION Inflammation EPIDERMIS DERMIS Chemical is recognized by Langerhans cells which then migrate from the skin to the draining lymph node Increased number of chemical-specific T-cells released into the systemic circulation This causes proliferation of specific T cells Lymph node Mature LC presents chemical to T cells D. Basketter

  19. Adverse Outcome Pathway (AOP) for Skin Sensitization In Silico, QSAR Reporter Gene (ARE) HRIPT/ Buehler DPRA h-CLAT LLNA Molecular properties Molecular Initiating Event Cellular Response Organ Response Organism Response Expression of cell surface markers and cytokines Dermal inflammation (after challenge) Penetration into the viable epidermis Covalent interaction with proteins Proliferation of T-cells in lymph nodes Electrophilic reactivity MHC II

  20. BASF Approaches sensitizer Bauch et al., Tox in Vitro 2011 nonsensitizer 1 Modified MUSST 2h-CLAT using THP-1 cells obtained from DSZM

  21. Tiered Testing Approach Example (BASF)

  22. Tiered Testing Approach (Kao)

  23. Tiered Testing Approach (P&G)

  24. Botanical Cosmetic Ingredients Could the KeratinoSens assay detect sensitizing chemicals in a botanical ingredient mixture? • Safety assessment challenging (molar conc. of some components may be unknown) • Cosmetic ingredients containing botanical extracts are formulated with solvents, preservatives, and generally less than 10% extract • We measured the activity of 3 known sensitizers neat and then “spiked” at 1%- 2% into 4 different botanical ingredients (each with a different excipient solvent system) 1. Gluteraldehyde(GA)- strong sensitizer 2. Dimethyl maleate (DM)- moderate sensitizer 3. Cinnamic aldehyde (CA) – moderate sensitizer • Activity of the spiked samples was measured and compared to the neat sensitizer and the unspiked botanical ingredient Study performed in collaboration with

  25. Sample Data & Conclusions • The sensitizer spike could be detected within the botanical ingredient (EC1.5 value) • Initial data suggests that the KS assay may be useful tool for the pre-clinical safety assessment of sensitization potential of botanical ingredients Botanical ingredient #2 w/o spike *No botanical ingredients showed sensitization potential w/o spike Botanical Matrix 2 –Gluteraldehyde 2% (MTT)  Conclusions

  26. Using In Vitro Assays, the Direct Peptide Reactivity Assay (DPRA), KeratinoSens™ Assay (KS), and Human Cell Line Activation Test (h-CLAT) to Assess Skin Sensitization Potential of Electronic Cigarette Liquids Presented at 2017 SOT Annual Meeting (Baltimore, MD) Two eCigarette liquids (non-sensitizers), spiked with cynnamic aldehyde (CA) (known sensitizer) to assess if the assays could detect sensitization potential in mixtures KeratinoSens and DPRA detection of sensitizer (at highest concentration of CA) More work need to be done with h-CLAT assay

  27. Considerations for Full Replacement using Available In Vitro, In Chemico, In Silico Methods • These assays do not currently address skin penetration & skin metabolism • Solubility is a concern • Assessment of Potency • Availability/Cost of methods • Best ITS is one that meets client goals • Screening (before clinical), submission?, timing, chemistry, etc. • Special Considerations • Mixtures (e.g. Botanicals) • Photo-activation • Assay Optimizations to address pro- haptens

  28. Recommended References • 1. Non-animal methods to predict skin sensitization (I): the Cosmetics Europe database Http://doi.org/10.1080/10408444.2018.1429385 • 2. Non-animal methods to predict skin sensitization(II): an assessment of defined approaches Http://doi.org10.1080/10408444.2018.1429386

  29. Acknowledgements • Givaudan • P&G • S.C. Johnson • Mary Kay • Merck • KeratinoSens ring trial participants (Givaudan, BASF, Beiersdorf, P&G) • LuSens ring trial participants (BASF, P&G, DSM, BRT) • The Clorox Company for funds for IIVS participation in KeratinoSens ring trial • Colgate-Palmolive Company for funds for IIVS participation in KeratinoSens ring trial • IIVS lab team

  30. Thank you for your attention Questions & Discussion

  31. References Basketter, D., Alepee, N., Casati, S., Crozier, J., Eigler, D., Griem, P., Hubesch, B., de, K.J., Landsiedel, R., Louekari, K., Manou, I., Maxwell, G., Mehling, A., Netzeva, T., Petry, T., Rossi, L.H., 2013. Skin sensitisation – moving forward with non-animal testing strategies for regulatory purposes in the EU. Regul. Toxicol. Pharmacol.67, 531–535. Basketter, D.A., Alepee, N., Ashikaga, T., Barroso, J., Gilmour, N., Goebel, C., Hibatallah, J., Hoffmann, S., Kern, P., Martinozzi-Teissier, S., Maxwell, G., Reisinger, K., Sakaguchi, H., Schepky, A., Tailhardat, M., Templier, M., 2014. Categorization of chemicals according to their relative human skin sensitizing potency. Dermatitis 25, 11–21 Bauch et al. (2012) Putting the parts together: Combining in vitro methods to test for skin sensitizing potentials. RegToxPharmacol 63(3):489-504 Bauch et al. (2011) Intralaboratory validation of four in vitro assays for the prediction of the skin sensitizing potential of chemicals. Toxicol In Vitro 25(6):1162-8. D. Gan, K. Norman, N. Barnes, H. Raabe, C. Gomez, and J. Harbell Application of the KeratinoSens Assay for Prediction of Dermal Sensitization Hazard for Botanical Cosmetic Ingredients. Presented at 2013 SOT Gerberick, F., Aleksic, M., Basketter, D., Casati, S., Karlberg, A.T., Kern, P., Kimber, I., Lepoittevin, J.P., Natsch, A., Ovigne, J.M., Rovida, C., Sakaguchi, H., Schultz, T., 2008. Chemical reactivity measurement and the predictive identification of skin sensitisers. Altern. Lab. Anim. 36, 215–242 Gerberick, G.F., Ryan, C.A., Kern, P., Schlatter, H., Dearman, R., Kimber, I., Patlewicz, G., Basketter, D., 2005. Compilation of historical local lymph node data for evalutaion of skin sensitization alternative methods. Dermatitis 16, 157–202 Gerberick, G.F., Vassallo, J.D., Bailey, R.E., Chaney, J.G., Morrall, S.W., Lepoittevin, J.P.,2004. Development of a peptide reactivity assay for screening contact allergens.Toxicol. Sci. 81, 332–343 Jaworska, JS, Natsch, A, ·Ryan, C,· Strickland, J, Ashikaga, T, · Miyazawa, M. Bayesian integrated testing strategy (ITS) for skin sensitization potency assessment: a decision support system for quantitative weight of evidence and adaptive testing strategy. Arch Toxicol 20 October 2015 DOI 10.1007/s00204-015-1634-2

  32. References Miller, et. al. Using In Vitro Assays, the Direct Peptide Reactivity Assay (DPRA), KeratinoSens™ Assay (KS), and Human Cell Line Activation Test (h-CLAT) to Assess Skin Sensitization Potential of Electronic Cigarette Liquids. Presented at 2017 SOT meeting NatschA., Emter R. Reporter cell lines for skin sensitization testing. Arch. Toxicol. 2015;89:1645–1648. doi: 10.1007/s00204-015-1555-0 Natsch A, Ryan CA, Foertsch L, Emter R, Jaworska J, Gerberick F, Kern P. A dataset on 145 chemicals tested in alternative assays for skin sensitization undergoing prevalidation. J ApplToxicol. 2013 Nov;33(11):1337-52. doi: 10.1002/jat.2868. Natsch, A., Bauch, C., Foertsch, L.M., Gerberick, G.F., Norman, K., Hilberer, H., Inglis, H., Landsiedel, R., Onken, S., Reuter, R., Schepky, A., Emter, R., 2011. The intra and inter-laboratory reproducibility and predictivity of the KeratinoSens assay to predict skin sensitizers in vitro: results of a ring-study in five laboratories. Toxicol. In Vitro 25, 733–744. OECD 2012a. The Adverse Outcome Pathway for Skin Sensitisation Initiated by Covalent Binding to Proteins. Part 1: Scientific Evidence. Series on Testing and Assessment No.168. OECD 2012b. The Adverse Outcome Pathway for Skin Sensitisation Initiated by Covalent Binding to Proteins. Part 2: Use of the AOP to Develop Chemical Categories and Integrated Assessment and Testing Approaches. Series on Testing and Assessment No. 168. ENV/JM/MONO(2012)10/PART2 OECD, (2015). Test No. 442C. In Chemico Skin Sensitization: Direct Peptide Reactivity Assay (DPRA). In OECD Guidelines for the Testing of Chemicals, Section 4: Health Effects, OECD Publishing OECD, (2015). Test No. 442D. In Vitro Skin Sensitisation: ARE-Nrf2 Luciferase Test Method. In OECD Guidelines for the Testing of Chemicals, Section 4: Health Effects, OECD Publishing OECD, (2016). Test No. 442E. In Vitro Skin Sensitisation: human Cell Line Activation Test (h-CLAT). In OECD Guidelines for the Testing of Chemicals, Section 4: Health Effects, OECD Publishing Otsubo, Y, Nishijo, T, Miyazawa, M, Saito, K, Mizumachi, H, Sakaguch, H. Binary test battery with KeratinoSens™ and h-CLAT as part of a bottom-up approach for skin sensitization hazard prediction. 2017. Regulatory Toxicology and Pharmacology 88 118-124. Wong, CL, Ghassabian, S, Smith MT, Lam A. In vitro methods for hazard assessment of industrial chemicals–opportunities and challenges. 2015. Frontiers in Pharmacology. doi:10.3389/fphar.2015.00094

More Related