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Immunotoxicology in Food and Ingredient Safety Assessment: Approaches and Case Studies
April 14, 2015
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Introduction to Immunology and Immunotoxicology Dori R. Germolec, Ph.D. Immunology Discipline Leader Toxicology Branch, National Toxicology Program National Institute for Environmental Health Sciences Research Triangle Park, North Carolina [email protected]
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Role of the Immune System in Homeostasis
Recognition and elimination of pathogenic organisms – Bacteria, viruses, fungi, parasites and their products
Recognition and elimination of neoplastic cells Response to foreign proteins
– Hypersensitivity responses
Distinguishes self from non-self – Breakage of tolerance to self – leads to autoimmunity
Regulation of the immune response once it has been initiated
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A System in Balance
Normal
Immunosuppression
Altered resistance to Infectious Disease
and Neoplasia
Immunostimulation
Hypersensitivity Autoimmunity
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Basics of Immunology The Immune Response
Innate (Non-specific) Immunity • Phylogenetically ancient • First line of defense • Rapid (minutes – hours) • Limited recognition • No cell proliferation required • Limited memory (? mammals)
Adaptive (Acquired) Immunity • Cell- and humoral-mediated immunity
T and B lymphocytes • Infinite array of specificities • Slow (days) • Requires proliferation and differentiation • Long-lasting memory
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Immune System Anatomy
BALT
NIH Publication No. 07-5423 September 2007; www.niaid.nih.gov
Primary Lymphoid Organs
– Bone Marrow – Thymus
Secondary Lymphoid Organs
– Spleen – Lymph Nodes – Peyer’s Patch
Tertiary Lymphoid Organs
– SALT, BALT, GALT, MALT
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Thymus size and architecture • Very sensitive to certain xenobiotics and drugs • Very sensitive to acute toxicity and stress
Images from NTP atlas of non-neoplastic lesions (http://ntp.niehs.nih.gov/nnl/)
Organs of the Immune System
Thymus: source of naive T cells
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Organs of the Immune System
Spleen: Antigen trapping and presentation, clonal expansion, cellular export
Image from NTP atlas of non-neoplastic lesions (http://ntp.niehs.nih.gov/nnl/)
Image courtesy of Dr. Jim Faix, Northern Arizona University
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Organs of the Immune System Lymph nodes: Antigen trapping and presentation,
clonal expansion, cellular export
Images from NTP atlas of non-neoplastic lesions (http://ntp.niehs.nih.gov/nnl/)
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Organs of the Immune System
Bone Marrow: Primary Source of Immune System Cells
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Neutrophil (“PMN”) • First responders • Phagocytosis and killing • of bacteria • Inflammation
Eosinophil • Allergy • Killing parasite larvae
Basophil • Circulating mast cells • Allergy/anaphylaxis • Resistance to intestinal • nematodes
Cells of the Innate Immune System: Granulocytes
Images courtesy of Dr. Michelle Cora, CMPB, NTP, NIEHS
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Cells of the Innate Immune System: Monocytes
Macrophage Phagocytosis
Monocyte/macrophage • Phagocytosis and killing of
bacteria • Antigen processing • Inflammation
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Inflammatory Mediators
• Eicosanoids • Hydrolytic Enzymes • Reactive Oxygen Species • Reactive Nitrogen Species • Adhesion Molecules • Cytokines and chemokines
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Main Features of Key Cytokines Source Cytokine Action Target
IFN γ T Cells Immunoregulation Lymphocytes Monocytes Antiviral
IL-1 Macrophages Immunoregulation T and B Cells Inflammation
Fever IL-2 T Cells Proliferation T and B Cells
Monocytes Activation
TNF α Macrophages Inflammation Fibroblast Cytotoxicity
IL-4 T Cells Division T and B Cells Differentiation
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Cells of the Innate Immune System: Dendritic Cells
• Intersection of innate and adaptive response • Identify threats via pattern recognition
receptors • Professional antigen presenting cells
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Cells of the Adaptive Immune System: B Lymphocytes
• B cells differentiate into plasma cells, secrete antibody: IgM, IgG, IgA, IgE - IgM: Primary response, efficient agglutination - IgG: Recall response, highest serum concentration - IgA: Mucosal surfaces, trapping of microbes - IgE: Parasitic infections, allergy, anaphylaxis
Heavy Chain
Light Chain
Antigen Binding Sites
(Fragment Crystallizable) Fc
Fab (Fragment Antigen Binding)
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Cells of the Adaptive Immune System: T Lymphocytes
• CD4+ T helper (Th) cells produce stimulatory and regulatory cytokines - Th1-cellular immunity/inflammation: IL-2, IFNγ, TNFβ - Th2-humoral immunity, resistance to helminths, allergy: IL-4, IL-5, IL-10, Il-13 - Th17-inflammation/resistance to infection and autoimmune disease: IL-17
• CD4+CD25+FoxP3+ T regulatory (Treg): downregulate autoreactive cells
• CD8+ T cytotoxic/suppressor (Ts/c): direct cytotoxicity, cytokine production
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Factors Affecting Immunocompetence
• Age • Sex • Genotype • Nutritional status • Life style choices
Immunocompetence, in the absence of chemical exposure, is complex, dynamic and affected by fixed and variable factors. Therefore, at the population level, the “normal” range is broad.
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Mechanisms of Resistance to Infectious Agents
Extracellular pathogens Staphylococcus, Streptococcus, E. coli,
viruses/parasites, microbial toxins
Humoral Immunity Antibody
Neutralization
Opsonization
Lysis
Intracellular pathogens Listeria, M. tuberculosis,
Leishmania, viruses
Cell Mediated Immunity Cytokine production
Activation of intra- cellular killing
Lysis
Susceptibility to infection is strongly correlated with immunocompetence and the type of immune system defect
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Nonimmmune Factors Influencing Outcome of Pathogen Encounter
Physical barriers • Skin, mucus lining, intestinal
motility
Microbicidal products • Fatty acids on skin • Lysozyme in tears, sweat • Acid environment of stomach
Competitive normal flora • Physical space • Inhibitory products/metabolites • Microbiome
Host Factors Dose of organism • Few: easily overcome • Many: Overwhelms innate defenses
Virulence factors • Toxins • Adherence factors • Evasion of host IR
- Mimic host proteins - Inhibit or disrupt IR
• Rapid growth • Very low infectious dose
- Norovirus, Giardia - Cryptosporidium
Pathogen Factors
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What happens when something goes wrong with the immune response?
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Adverse Immune Responses
• Immunomodulation - Immunosuppression - Immunostimulation
• Hypersensitivity • Autoimmunity
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The NTP Immunotoxicology Testing Paradigm
• How do we evaluate for immunosuppression or immunostimulation after chemical exposure?
- Basic Toxicology - Immune Function Assays - Host Resistance Assays
• May be assessed following adult or developmental exposures (sometimes both)
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Development of a testing battery to assess chemical-induced immunotoxicity: National Toxicology Program’s Guidelines for Immunotoxicity Evaluation in Mice
Luster et al. Fundamental and Applied Toxicology 10: 2-19 (1988) Screen (Tier I)
– Immunopathology (Hematology, Organ weights, Spleen Cellularity, Histopathology)
– Humoral Immunity (IgM TDAR; Proliferative Responses – LPS) – Cell-mediated Immunity (Proliferative responses – MLR, ConA) – Non-specific Immunity (NK cell assay)
Comprehensive (Tier II) – Cell Quantification (Surface Marker Analysis in spleen) – Humoral Immunity (IgG TDAR) – Cell-mediated Immunity (CTL, DTH) – Non-specific Immunity (Macrophage Function) – Host resistance assays
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p<.0001
p<.0014
p<.0003
p<.0458
p<.0348
p<.2380
p<.0017
p<.4490
p<.0009
p<.0395
p<.0694
p=.2260
78 (45)
94 (34)
85 (40)
82 (34)
89 (27)
100 (8)
91 (23)
86 (28)
92 (38)
85 (39)
80 (35)
81 (37)
69 (36)
79 (34)
74 (31)
84 (19)
78 (9)
90 (21)
71 (24)
81 (31)
75 (32)
72 (29)
73 (30)
67 (46)
73 (37)
82 (28)
71 (7)
92 (24)
62 (29)
83 (36)
76 (37)
72 (32)
69 (39)
56 (39)
57 (30)
74 (23)
75 (8)
- (0)
67 (9)
87 (23)
93 (14)
100 (5)
83 (24)
59 (27)
67 (18)
67 (6)
80 (20)
43 (30)
77 (30)
75 (24)
71 (7)
90 (21)
72 (29)
68 (40)
65 (31)
71 (24)
75 (8)
86 (22)
62 (29)
73 (40)
61 (41)
63 (30)
67 (21)
71 (7)
76 (21)
60 (25)
75 (32)
63 (32)
56 (36)
65 (31)
58 (24)
83 (6)
56 (27)
74 (34)
71 (35)
63 (27)
50 (40)
90 (20)
Plaque Forming Cells
NK Cell Activity
T Cell Mitogens
MLR
DHR
CTL
Surface Markers
Leukocyte Counts
Thymus/BW Ratio
Spleen/BW Ratio
Spleen Cellularity
LPS Response
p<.0001
p<.0014
p<.0003
p<.0458
p<.0348
p<.2380
p<.0017
p<.4490
p<.0009
p<.0395
p<.0694
p=.2260
78 (45)
69 (36)
67 (46)
56 (39)
57 (30)
67 (9)
83 (24)
43 (30)
68 (40)
61 (41)
56 (36)
50 (40)
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IL-1
T cell
IL-2
Macrophage
B cell
IL-2, IL-4, IL-5
Plasma cell
T DTH
T CTL
Antigen
CD4
Ig
Ig
CD4
CD8
Why is the T-dependent antibody response highly predictive?
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Complement + sRBC in Agar Solution
3 Hour Incubation
Magnified
500 µl Aliquot
Sheep RBC (AFC)
sRBC around AFC
PLAQUE are hemolyzed =
Antibody Forming Cell
IgM Plaque Forming Cell Assay
Day 4
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Kinetics of the Antibody Response
.
Secondary Antigen Challenge
Primary Antigen Challenge
Time (days)
40 32 16 8 24 0
IgG IgM
Seru
m A
ntib
ody
Tite
r
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p<.0001
p<.0014
p<.0003
p<.0458
p<.0348
p<.2380
p<.0017
p<.4490
p<.0009
p<.0395
p<.0694
p=.2260
78 (45)
94 (34)
85 (40)
82 (34)
89 (27)
100 (8)
91 (23)
86 (28)
92 (38)
85 (39)
80 (35)
81 (37)
69 (36)
79 (34)
74 (31)
84 (19)
78 (9)
90 (21)
71 (24)
81 (31)
75 (32)
72 (29)
73 (30)
67 (46)
73 (37)
82 (28)
71 (7)
92 (24)
62 (29)
83 (36)
76 (37)
72 (32)
69 (39)
56 (39)
57 (30)
74 (23)
75 (8)
- (0)
67 (9)
87 (23)
93 (14)
100 (5)
83 (24)
59 (27)
67 (18)
67 (6)
80 (20)
43 (30)
77 (30)
75 (24)
71 (7)
90 (21)
72 (29)
68 (40)
65 (31)
71 (24)
75 (8)
86 (22)
62 (29)
73 (40)
61 (41)
63 (30)
67 (21)
71 (7)
76 (21)
60 (25)
75 (32)
63 (32)
56 (36)
65 (31)
58 (24)
83 (6)
56 (27)
74 (34)
71 (35)
63 (27)
50 (40)
90 (20)
Plaque Forming Cells
NK Cell Activity
T Cell Mitogens
MLR
DHR
CTL
Surface Markers
Leukocyte Counts
Thymus/BW Ratio
Spleen/BW Ratio
Spleen Cellularity
LPS Response
p<.0001
p<.0014
p<.0003
p<.0458
p<.0348
p<.2380
p<.0017
p<.4490
p<.0009
p<.0395
p<.0694
p=.2260
78 (45)
69 (36)
67 (46)
56 (39)
57 (30)
67 (9)
83 (24)
43 (30)
68 (40)
61 (41)
56 (36)
50 (40)
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Current testing battery to assess chemical-induced immunotoxicity: National Toxicology Program’s Guidelines for Immunotoxicity Evaluation in Rodents
Screen (Tier I) – Immunopathology (Hematology, Organ weights, Spleen Cellularity,
Histopathology) – Cell Quantification (Surface Marker Analysis in spleen) – Humoral Immunity (IgM TDAR) – Cell-mediated Immunity (CTL, DTH) – Non-specific Immunity (NK cell assay)
Definitive (Tier II) – Humoral Immunity (IgG TDAR) – Non-specific Immunity (Macrophage Function) – Host resistance assays
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Disease Resistance Models to Evaluate Immunomodulatory Effects
Challenge Agent Endpoint Measured Listeria monocytogenes Liver, CFU, Spleen CFU, Morbidity Strep pneumoniae Morbidity Plasmodium yoelli Parasitemia Influenza Virus Morbidity, Viral titer/tissue burden Cytomegalovirus Morbidity, Viral titer/tissue burden Trichinella spiralis Encysted larvae, Adult parasites PYB6 Sarcoma Tumor Incidence (subcutaneous) B16F10 Melanoma Tumor Burden (Lung nodules)
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Decreased Host Resistance: Implications for Human Health
• Most likely adverse outcome in humans is mild to moderate immunosuppression - Consequences: decreased resistance to common
infections • Redundancy and reserve capacity compromised
- At the population level • Small but potentially significant increase in incidence or severity
of disease • Significant economic impact
- At the individual level • Outcome dependent on response phenotype, xenobiotic dose,
encounter with infectious agent
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Assessment of Immunocompetence in Humans
• Hematology • Clinical Chemistry • Serum Immunoglobulins • Surface Markers • Proliferation of PBLs • Macrophage Assays • Primary or Secondary antibody responses to vaccines • Health Histories - Self or physician reported infectious
disease or neoplasia rates
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In Vitro Studies
• A majority of the in vivo/ ex vivo tests have an in vitro counterpart
• In vitro studies often excellent for providing mechanistic or mode of action information
• Have been a number of efforts to validate in vitro endpoints with functional immune tests
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Adverse Immune Responses
• Immunomodulation • Hypersensitivity • Autoimmunity
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Coombs and Gell Classification of Hypersensitivity Responses
Type Reaction
I
II
III
IV
Immediate (IgE)
Antibody-dependent cytotoxic
Immune-complexes
Delayed type (DTH)
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• Guinea Pig Tests - Maximization Test
- Occlusive Patch Test
- Respiratory Challenge
- Systemic Anaphylaxis
• Murine Local Lymph Node Assay
• Mouse Ear Swelling Test
Models for Assessing Dermal Sensitization
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Local Lymph Node Assay 125IUDR
DNFB
3 Days
Rest 2 Days
Rest 5 Hours
Excise Lymph Nodes
Process Nodes
Count DPMs
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Adverse Immune Responses
• Immunomodulation • Hypersensitivity • Autoimmunity
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Autoimmunity is an inappropriate immune response against self-antigens
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Spectrum of Autoimmune Diseases and Putative Autoantigens
Hashimoto’s Thyroiditis Thyrotoxicosis Pernicious anemia Autoimmune Atrophic Gastritis Addison’s Disease Insulin-Dependent Diabetes Mellitus Goodpasture’s Syndrome Myasthenia Gravis Male Infertility (isolated cases) Sympathetic Ophthalmia Multiple Sclerosis Autoimmune Hemolytic Anemia Ulcerative Colitis Rheumatoid Arthritis Scleroderma Systemic Lupus Erythematosus (SLE)
Thyroglobulin Thyroid-stimulating hormone (TSH) H+/K+-ATPase Intrinsic factor 21-hydroxylase Glutamic acid decarboxylase 65 Type IV collagen Acetyl choline receptor Epididymal glycoprotein, FA-1 Interphotoreceptor retinol binding protein Myelin basic protein X-antigen, glycophorin Catalase; a-enolase Rheumatoid factor Topoisomerase 1; laminins DNA nucleotides and histones
Organ Specific
Non-Organ Specific
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Modulation of genetic or experimentally-induced autoimmunity can be measured:
• In humans and experimental animals - Quantitation of autoantibody levels - Measurement of tissue cytokine and cytokine receptor
levels - Measurment of appropriate and serum or urinary
parameters • In experimental animals only
- Histologic evaluation of tissue damage - Popliteal lymph node assay
Methods to assess Autoimmunity
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Animal Models • Genetic Predisposition
• Insulin-Dependent Diabetes Mellitus - NOD (m), BB (r), BN (r)
• Systemic Lupus Erythematosus - MRL+/+ (m), MRL/lpr (m), NZB/NZW (m)
• Autoimmunization • Multiple Sclerosis
- CFA + myelin basic protein (m,mo) • Organic or Chemical Induction
• Systemic Lupus Erythematosus - Mercury (m,r,mo) - Penicillamine (m,r) - Procainamide (m.r)
Methods to Study Autoimmune Disease
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How do we evaluate the data once we have obtained it?
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Exposure to a single agent or class of chemicals is very unlikely
Challenges
• Long latency period between
exposure and onset of disease • “No effects” tough to prove
– Must distinguish no response in individual vs. no effects in the population
– Small numbers of subjects – Determining true dose is difficult
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NTP Levels of Evidence Criteria The NTP has long employed specific conclusion statements, that are
approved by the NTP BSC, for its “Toxicology and Carcinogenesis” studies
The NTP has developed similar conclusion statements to represent a “level of evidence” with regard to evaluating immune system toxicity
– Clear evidence – Some evidence – Equivocal evidence – No evidence – Inadequate study
Such an approach allows for comparisons of different studies on the same test substance and for comparisons of conclusions across studies, to ensure similar criteria are employed uniformly
The NTP has developed guidance notes as to how these criteria should be applied
http://ntp.niehs.nih.gov/testing/types/criteria/index.html
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Weight of Evidence Approach to Hazard Identification
• Guidance Contains Distinct Flow Charts for Immunosuppression, Immunomodulation, Hypersensitivity and Autoimmunity
• Questions prioritized from most predictive to least
• Vary slightly depending on what risk is being considered
Organ weight data are equivocal evidence of immunosuppression.
Observational immune assays generally present equivocal evidence of immunosuppression.
GO TO QUESTION #5.
Haematological data generally present equivocal evidence of immunosuppression.
GO TO QUESTION #6.
Immune function data represent clear evidence of adverse immunosuppression.
GO TO QUESTION #4.
Host resistance data represent clear evidence of adverse immunosuppression.
GO TO QUESTION #3.
Well-controlled clinical and epidemiological studies represent clear evidence of adverse immunosuppression.
GO TO QUESTION #2.
Histopathological data generally present equivocal evidence of immunosuppression. GO TO QUESTION #7.
QUESTION 2: Is there evidence that the chemical causes increased incidences infections and or tumors?
Develop WoE conclusions for immunosuppression hazard ID based on answers to all 7 questions.
QUESTION 4: Is there evidence from general or observational immune assays (lymphocyte phenotyping, cytokines, complement, lymphocyte proliferation, etc.) that the chemical is immunosuppressive?
QUESTION 3: Is there evidence that the chemical reduces immune function (antibody production, NK cell function, DTH, MLR, CTL, phagocytosis or bacterial killing by monocytes, etc.)?
QUESTION 5: Is there evidence that the chemical causes haematological changes (e.g. altered WBC counts) suggestive of immune effects?
QUESTION 7: Is there evidence that the chemical reduces immune organ weight (thymus, spleen, lymph nodes, etc.)?
QUESTION 1: Are there epidemiological studies, clinical studies or case-studies available that provide human data on end-points relevant to immuno-suppression (i.e. incidence of infections, response to vaccination, DTH, lymphocyte proliferation, other data)?
QUESTION 6: Is there histopathological evidence (thymus, spleen, lymph nodes, etc.) that suggests that the chemical causes immunotoxicity?
From the WHO Harmonization Project – GUIDANCE FOR IMMUNOTOXICITY RISK ASSESSMENT FOR CHEMICALS. Available on the WHO website: http://www.who.int/ipcs/en/
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Case studies illustrating adverse immune responses
• Immunomodulation – Dr. Jamie DeWitt, Immunomodulatory Effects of Perfluoroalkyl Substances in Rodents and Humans
• Hypersensitivity – Toxicology and Food Allergy: Case study of the food preservative, tBHQ
• Autoimmunity – Dr. Prakash Nagarkatti, Dietary Supplement Modulation of Autoimmune Disease
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