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Anti-Aflatoxin
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Aflatoxin Antibodies

Aflatoxins are highly toxic and carcinogenic compounds produced by molds like Aspergillus flavus and Aspergillus parasiticus, typically found in foods such as peanuts, corn, and tree nuts. 

These mycotoxins, particularly aflatoxin B1, are among the most potent natural carcinogens, capable of causing liver cancer, immune suppression, and stunted growth in children. 

Aflatoxins persist in food and animal feed even after processing, posing ongoing health risks. Chronic exposure leads to bioaccumulation in the liver, increasing the potential for severe health outcomes. 

Detecting and managing aflatoxin contamination is crucial for ensuring food safety and public health.

What are Aflatoxins?  [7.] 

Aflatoxins are a group of highly toxic and carcinogenic compounds produced as secondary metabolites by certain molds, primarily Aspergillus flavus and Aspergillus parasiticus.  [7., 17.]

They are one type of mycotoxin, which are a larger group of toxic chemical compounds produced by molds.  

These mycotoxins are formed when the molds colonize foods like peanuts, corn, cottonseed, tree nuts, and spices under favorable temperature and humidity conditions.   [7., 16.] 

The main aflatoxins are B1, B2, G1, and G2, with aflatoxin B1 (AFB1) being the most potent and carcinogenic.  [3.] 

Their production occurs when the mold's growth is stressed, such as during drought conditions or improper crop storage. 

Aflatoxins are among the most carcinogenic substances known - they can cause acute toxicity leading to liver failure, hemorrhaging, and even death in severe cases.   [7.]  Chronic exposure increases the risk of developing liver cancer, as aflatoxins can bind to DNA and cause mutations, particularly in the p53 tumor suppressor gene. [7., 9.]

They can also suppress the immune system, and can cause stunted growth in children.  [8., 12., 13.] 

Worryingly, aflatoxins are highly stable and can persist in foods and animal feeds even after processing and cooking.  They bioaccumulate in the body over time, especially in the liver, due to their lipophilic nature and resistance to metabolic breakdown.  [1., 10., 11.] 

Aflatoxin B1 is metabolized to the reactive aflatoxin-8,9-epoxide, which binds to DNA and proteins, initiating carcinogenesis.  [13.] 

Animals fed contaminated feed can pass aflatoxin metabolites into meat, milk, and eggs, posing risks to humans consuming these products.

Anti-Aflatoxin Biomarkers

Anti-aflatoxin biomarkers are a group of compounds or metabolites that can be measured in biological samples to assess exposure to aflatoxins, which are toxic and carcinogenic metabolites produced by certain molds. 

These biomarkers provide a direct measure of internal exposure and can help evaluate the associated health risks.

A variety of biomarkers have been used to identify the presence of aflatoxins in humans and animals.  

Aflatoxin-Albumin Adducts  [7., 16., 17.]

One of the most widely used anti-aflatoxin biomarkers is the aflatoxin-albumin adduct (AF-alb).  AF-alb is formed by the metabolic activation of aflatoxin B1 (AFB1) and its subsequent binding to albumin in the blood. 

It serves as a reliable biomarker of integrated AFB1 exposure over the previous 2-3 months. 

AF-alb is measured using immunoassays like ELISA or LC-MS/MS methods.

Urinary Aflatoxin M1 (AFM1)  [7.] 

AFM1 is a hydroxylated metabolite of AFB1 that is excreted in urine.  Its measurement reflects recent AFB1 exposure over the past 24-48 hours. 

AFM1 levels in urine are analyzed by immunoassays or LC-MS/MS.

Urinary Aflatoxin-N7-Guanine (AF-N7-Gua)  [7., 16., 17.] 

AF-N7-Gua is a product of AFB1 binding to DNA, forming adducts.  Its measurement in urine indicates the biologically effective dose of AFB1 that has led to DNA damage. 

AF-N7-Gua is typically analyzed using LC-MS/MS methods.

Aflatoxin B1, B2, G1, G2

Testing for aflatoxins, particularly aflatoxin B1, B2, G1, and G2, has significant clinical utility in assessing exposure and potential health risks. 

Aflatoxin B1 is one of the most potent naturally occurring carcinogens and is strongly linked to the development of hepatocellular carcinoma (liver cancer), especially in individuals with chronic hepatitis B or C infections.  [2.] 

Measuring aflatoxin levels in food, feed, and biological samples like blood or urine can help identify exposure sources and quantify the extent of exposure. 

This information is crucial for risk assessment, implementing preventive measures, and monitoring the effectiveness of interventions aimed at reducing aflatoxin contamination. 

Additionally, aflatoxin testing plays a vital role in food safety and regulatory compliance, as many countries have established maximum permissible limits for these toxins in various food products to protect public health.  Accurate and sensitive analytical methods for aflatoxin detection are essential for enforcing these regulations and ensuring the safety of the food supply chain.

Aflatoxin Q1 (AFQ1) and aflatoxin P1 (AFP1)  [7., 17.]

These are minor metabolites of AFB1 that can be measured in urine as additional biomarkers of recent exposure.

Anti-Aflatoxin Laboratory Testing Methods

Test Information, Sample Collection and Preparation

Various biological samples can be employed to detect and quantify anti-aflatoxin biomarkers, particularly blood, urine and nasal secretions.

Blood samples are typically collected via venipuncture in a clinical setting, while urine and nasal secretion samples may be collected from the comfort of home.  

It is important to consult with the ordering provider prior to sample collection, as certain protocols may be recommended beforehand.  

Interpretation of Anti-Aflatoxin Test Results

Optimal Levels of Anti-Aflatoxin Test Results

Because of the high level of toxicity of aflatoxins, optimal test results indicate undetectable levels of aflatoxins.  

Clinical Significance of Elevated Aflatoxins

Elevated levels of aflatoxins indicate recent or current exposure to aflatoxins.  However, because they are known to bioaccumulate, testing positive for the presence of aflatoxins may indicate a persistent historical exposure.  [4., 5., 15.] 

Clinical Significance of Low Aflatoxins

Low or undetectable levels of aflatoxins are considered ideal.  

Anti-Aflatoxin Related Biomarkers

In addition to the direct measurement of anti-aflatoxin biomarkers, other biomarkers can provide complementary information about aflatoxin exposure and its potential health effects.

Oxidative Stress Markers  [14., 18.]

Aflatoxin exposure is known to induce oxidative stress, which can lead to cellular damage and contribute to the development of various diseases. 

Biomarkers such as malondialdehyde (MDA) and 8-hydroxy-2'-deoxyguanosine (8-OHdG) can be measured to assess oxidative stress levels and the associated risk of aflatoxin-related toxicity.  [14.] 

Liver Function Markers  [6.] 

Since the liver is a primary target organ for aflatoxin toxicity, monitoring liver function biomarkers like alanine aminotransferase (ALT), aspartate aminotransferase (AST), and bilirubin can provide insights into the extent of hepatic injury and potential liver damage caused by aflatoxin exposure.  

Inflammatory Biomarkers  [14.] 

Aflatoxin exposure can trigger inflammatory responses, and biomarkers such as C-reactive protein (CRP), interleukins (e.g., IL-6, IL-8), and tumor necrosis factor-alpha (TNF-α) can be measured to evaluate the inflammatory status and associated health risks.

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See References

[1.] Bansal A, Sharma M, Pandey A, Shankar J. Aflatoxins: Occurrence, Biosynthesis Pathway, Management, and Impact on Health. Fungal Resources for Sustainable Economy. Published online 2023:565-594. doi:https://doi.org/10.1007/978-981-19-9103-5_21

[2.] Chen CH, Wang MH, Wang JH, et al. Aflatoxin Exposure and Hepatitis C Virus in Advanced Liver Disease in a Hepatitis C Virus–Endemic Area in Taiwan. American Journal of Tropical Medicine and Hygiene. 2007;77(4):747-752. doi:https://doi.org/10.4269/ajtmh.2007.77.747

[3.] Dai C, Tian E, Hao Z, Tang S, Wang Z, Sharma G, Jiang H, Shen J. Aflatoxin B1 Toxicity and Protective Effects of Curcumin: Molecular Mechanisms and Clinical Implications. Antioxidants (Basel). 2022 Oct 14;11(10):2031. doi: 10.3390/antiox11102031. PMID: 36290754; PMCID: PMC9598162.

[4.] Ferri F, Brera C, De Santis B, Collini G, Crespi E, Debegnach F, Gargano A, Gattei D, Magnani I, Mancuso P, Mozzanica S, Teodori E, Djuric O, Giorgi Rossi P. Association between Urinary Levels of Aflatoxin and Consumption of Food Linked to Maize or Cow Milk or Dairy Products. Int J Environ Res Public Health. 2020 Apr 6;17(7):2510. doi: 10.3390/ijerph17072510. PMID: 32268619; PMCID: PMC7177871.

[5.] Gong YY, Watson S, Routledge MN. Aflatoxin Exposure and Associated Human Health Effects, a Review of Epidemiological Studies. Food Safety. 2016;4(1):14-27. doi:https://doi.org/10.14252/foodsafetyfscj.2015026

[6.] Güç, İ., Yalçin, E., Çavuşoğlu, K. et al. Toxicity mechanisms of aflatoxin M1 assisted with molecular docking and the toxicity-limiting role of trans-resveratrol. Sci Rep 12, 14471 (2022). https://doi.org/10.1038/s41598-022-18791-8

[7.] International Agency For Research On Cancer. Working Group On The Evaluation Of The Carcinogenic Risks To Humans. Some Traditional Herbal Medicines, Some Mycotoxins, Naphthalene and Styrene : This Publication Represents the Views and Expert Opinions of an IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, Which Met in Lyon, 12-19 February 2002. Iarc; 2002.

[8.] Jiang Y, Jolly PE, Preko P, Wang JS, Ellis WO, Phillips TD, Williams JH. Aflatoxin-related immune dysfunction in health and in human immunodeficiency virus disease. Clin Dev Immunol. 2008;2008:790309. doi: 10.1155/2008/790309. PMID: 18695741; PMCID: PMC2496958.

[9.] Kew MC. Aflatoxins as a cause of hepatocellular carcinoma. J Gastrointestin Liver Dis. 2013 Sep;22(3):305-10. PMID: 24078988.

[10.] Kumar P, Mahato DK, Kamle M, Mohanta TK, Kang SG. Aflatoxins: A Global Concern for Food Safety, Human Health and Their Management. Front Microbiol. 2017 Jan 17;7:2170. doi: 10.3389/fmicb.2016.02170. PMID: 28144235; PMCID: PMC5240007.

[11.] MANCINI A, DREASSI E, BOTTA M, TARCHI F, FRANCARDI V. BIOACCUMULATION RISK ASSESSMENT OF AFLATOXIN B1, OCHRA-TOXIN AND FUMONISIN B1 IN TENEBRIO MOLITOR LARVAE. Redia. 2020;103:101-108. doi:https://doi.org/10.19263/redia-103.20.16

[12.] Mao Y, Dang M, Zhang J, et al. Peptide amphiphile inspired self-assembled, ordered gold nanocomposites for improved sensitivity of electrochemical immunosensor: Applications in determining the total aflatoxin amount in food stuffs. Talanta. 2022;247:123532-123532. doi:https://doi.org/10.1016/j.talanta.2022.123532

[13.] Mutocheluh M, Narkwa PW. Aflatoxin B1: An Immunomodulator and Cancer Agent. www.intechopen.com. Published November 30, 2022. https://www.intechopen.com/chapters/83715‌

[14.] Peng T, Li LQ, Peng MH, et al. Evaluation of oxidative stress in a group of adolescents exposed to a high level of aflatoxin B1 a multi-center and multi-biomarker study. Carcinogenesis. 2007;28(11):2347-2354. doi:https://doi.org/10.1093/carcin/bgm193

[15.] Tong Y, Tonui P, Orang'o O, Zhang J, Maina T, Muthoka K, Groopman J, Smith J, Madeen E, Ermel A, Loehrer P, Brown D. Association of Plasma Aflatoxin With Persistent Detection of Oncogenic Human Papillomaviruses in Cervical Samples From Kenyan Women Enrolled in a Longitudinal Study. Res Sq [Preprint]. 2023 Jan 27:rs.3.rs-2468599. doi: 10.21203/rs.3.rs-2468599/v1. Update in: BMC Infect Dis. 2023 Jun 6;23(1):377. PMID: 36747756; PMCID: PMC9901024.

[16.] Turner PC, Snyder JA. Development and Limitations of Exposure Biomarkers to Dietary Contaminants Mycotoxins. Toxins (Basel). 2021 Apr 28;13(5):314. doi: 10.3390/toxins13050314. PMID: 33924868; PMCID: PMC8147022.

[17.] Xu Y, Gong YY, Routledge MN. Aflatoxin exposure assessed by aflatoxin albumin adduct biomarker in populations from six African countries: REVIEW ARTICLE. World Mycotoxin J. 2018;11(3):411-419. doi: 10.3920/WMJ2017.2284. Epub 2018 Aug 1. PMID: 33552312; PMCID: PMC7797627.

[18.] Xue M, Fu M, Zhang M, et al. Aflatoxin B1 Induced Oxidative Stress and Gut Microbiota Disorder to Increase the Infection of Cyprinid Herpesvirus 2 in Gibel Carp (Carassius auratus gibelio). Antioxidants. 2023;12(2):306-306. doi:https://doi.org/10.3390/antiox12020306

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