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CH Instruments chi-2
Anti-MAA, anti-AGE, anti-CarP, and anti-AL antibodies are increased in patients with AILD, and especially in patients with <t>AIH.</t> IgG antibody levels are presented as arbitrary units per milliliter (aU/mL) and cut-off for each PTM is indicated by the dashed line. * p < 0.05, ** p < 0.01. Autoimmune Liver Disease: AIH, PBC and PSC; non-Autoimmune Liver Disease: NAFLD, HCV, HBV, ALD, Combination, NASH. AGE, advanced glycation end-product; AIH, autoimmune hepatitis; AL, acetylated protein; CarP, carbamylated protein; Cit, citrullinated protein; MAA, malondialdehyde–acetaldehyde adduct; ns, not significant; NT, nitrated protein.
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Anwendung GmbH vereinfachten aih-scores
Anti-MAA, anti-AGE, anti-CarP, and anti-AL antibodies are increased in patients with AILD, and especially in patients with <t>AIH.</t> IgG antibody levels are presented as arbitrary units per milliliter (aU/mL) and cut-off for each PTM is indicated by the dashed line. * p < 0.05, ** p < 0.01. Autoimmune Liver Disease: AIH, PBC and PSC; non-Autoimmune Liver Disease: NAFLD, HCV, HBV, ALD, Combination, NASH. AGE, advanced glycation end-product; AIH, autoimmune hepatitis; AL, acetylated protein; CarP, carbamylated protein; Cit, citrullinated protein; MAA, malondialdehyde–acetaldehyde adduct; ns, not significant; NT, nitrated protein.
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AstraZeneca ltd chadox1
A brief summary of studies addressing immune and autoimmune side effects of COVID-19 vaccines.
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MyoLearn electromyography (emg) research
A brief summary of studies addressing immune and autoimmune side effects of COVID-19 vaccines.
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Custo Med GmbH regressão simples
A brief summary of studies addressing immune and autoimmune side effects of COVID-19 vaccines.
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aih  (Moderna)
86
Moderna aih
A brief summary of studies addressing immune and autoimmune side effects of COVID-19 vaccines.
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BioNTech bnt162b2 mrna
Updated RUCAM for the hepatocellular injury of DILI and HILI RUCAM: Roussel Uclaf Causality Assessment Method scale; DILI: Drug-induced liver injury; HILI: Herb-induced liver injury (HILI) [ <xref ref-type= 17 ] * Group I (7 causes) HAV: Anti-HAV-IgM, Hepatobiliary sonography/color Doppler, HCV: Anti-HCV, HCV-RNA, HEV: Anti-HEV-IgM, anti-HEV-IgG, HEV-RNA, Hepatobiliary sonography/color Doppler sonography of liver vessels/ endo-sonography/CT/MRC, Alcoholism (AST/ALT ≥ 2), Acute recent hypotension history (particularly if underlying heart disease), *Group II (5 causes) Complications of underlying disease(s) such as sepsis, metastatic malignancy, autoimmune hepatitis, chronic hepatitis B or C, primary biliary cholangitis or sclerosing cholangitis, genetic liver diseases, Infection suggested by PCR and titer change for; CMV (anti-CMV-IgM, anti-CMV-IgG), EBV (anti-EBV-IgM, anti-EBV-IgG), HSV (anti-HSV-IgM, anti-HSV-IgG), VZV (anti-VZV-IgM, anti-VZV-IgG). **Patient's ALT 689 U/L, Upper limit of normal ALT 40 U/L, Patient's ALP 213 U/L, Upper limit of normal ALP 120 U/L, R-value 9.7, RUCAM score > 5. The hepatocellular pattern of liver injury. Recommend acute viral hepatitis serologies, HCV RNA and autoimmune hepatitis serologies, and imaging studies such as abdominal ultrasound) [ 18 ]." width="250" height="auto" />
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Image Search Results


Anti-MAA, anti-AGE, anti-CarP, and anti-AL antibodies are increased in patients with AILD, and especially in patients with AIH. IgG antibody levels are presented as arbitrary units per milliliter (aU/mL) and cut-off for each PTM is indicated by the dashed line. * p < 0.05, ** p < 0.01. Autoimmune Liver Disease: AIH, PBC and PSC; non-Autoimmune Liver Disease: NAFLD, HCV, HBV, ALD, Combination, NASH. AGE, advanced glycation end-product; AIH, autoimmune hepatitis; AL, acetylated protein; CarP, carbamylated protein; Cit, citrullinated protein; MAA, malondialdehyde–acetaldehyde adduct; ns, not significant; NT, nitrated protein.

Journal: Frontiers in Medicine

Article Title: Antibodies against multiple post-translationally modified proteins aid in diagnosis of autoimmune hepatitis and associate with complete biochemical response to treatment

doi: 10.3389/fmed.2023.1195747

Figure Lengend Snippet: Anti-MAA, anti-AGE, anti-CarP, and anti-AL antibodies are increased in patients with AILD, and especially in patients with AIH. IgG antibody levels are presented as arbitrary units per milliliter (aU/mL) and cut-off for each PTM is indicated by the dashed line. * p < 0.05, ** p < 0.01. Autoimmune Liver Disease: AIH, PBC and PSC; non-Autoimmune Liver Disease: NAFLD, HCV, HBV, ALD, Combination, NASH. AGE, advanced glycation end-product; AIH, autoimmune hepatitis; AL, acetylated protein; CarP, carbamylated protein; Cit, citrullinated protein; MAA, malondialdehyde–acetaldehyde adduct; ns, not significant; NT, nitrated protein.

Article Snippet: We did not observe a significant difference in the presence of anti-PTM antibodies in patients positive or negative for ANA or SMA, with the exception of anti-MAA positivity and ANA positivity in patients with AIH (Chi-2 (1) > = 4.687, p = 0.030).

Techniques:

Patients with AILD, and especially AIH, are more likely to be positive for more than one anti-PTM antibody. Data is presented as percentage positive (%) patients for a number of anti-PTM antibodies in (from left to right) healthy controls, non-autoimmune liver disease autoimmune liver disease and autoimmune hepatitis.

Journal: Frontiers in Medicine

Article Title: Antibodies against multiple post-translationally modified proteins aid in diagnosis of autoimmune hepatitis and associate with complete biochemical response to treatment

doi: 10.3389/fmed.2023.1195747

Figure Lengend Snippet: Patients with AILD, and especially AIH, are more likely to be positive for more than one anti-PTM antibody. Data is presented as percentage positive (%) patients for a number of anti-PTM antibodies in (from left to right) healthy controls, non-autoimmune liver disease autoimmune liver disease and autoimmune hepatitis.

Article Snippet: We did not observe a significant difference in the presence of anti-PTM antibodies in patients positive or negative for ANA or SMA, with the exception of anti-MAA positivity and ANA positivity in patients with AIH (Chi-2 (1) > = 4.687, p = 0.030).

Techniques:

The association between the presence of anti-PTM antibodies in HC, non-AILD,  AIH  and cholestatic liver disease.

Journal: Frontiers in Medicine

Article Title: Antibodies against multiple post-translationally modified proteins aid in diagnosis of autoimmune hepatitis and associate with complete biochemical response to treatment

doi: 10.3389/fmed.2023.1195747

Figure Lengend Snippet: The association between the presence of anti-PTM antibodies in HC, non-AILD, AIH and cholestatic liver disease.

Article Snippet: We did not observe a significant difference in the presence of anti-PTM antibodies in patients positive or negative for ANA or SMA, with the exception of anti-MAA positivity and ANA positivity in patients with AIH (Chi-2 (1) > = 4.687, p = 0.030).

Techniques:

Percentage of positivity for anti-PTM antibodies in ANA positive, ANA negative, SMA positive, SMA negative and double negative  (ANA  and SMA) patients with  AIH.

Journal: Frontiers in Medicine

Article Title: Antibodies against multiple post-translationally modified proteins aid in diagnosis of autoimmune hepatitis and associate with complete biochemical response to treatment

doi: 10.3389/fmed.2023.1195747

Figure Lengend Snippet: Percentage of positivity for anti-PTM antibodies in ANA positive, ANA negative, SMA positive, SMA negative and double negative (ANA and SMA) patients with AIH.

Article Snippet: We did not observe a significant difference in the presence of anti-PTM antibodies in patients positive or negative for ANA or SMA, with the exception of anti-MAA positivity and ANA positivity in patients with AIH (Chi-2 (1) > = 4.687, p = 0.030).

Techniques:

Characteristics of untreated  AIH  patients in the AILD cohort ( n = 58).

Journal: Frontiers in Medicine

Article Title: Antibodies against multiple post-translationally modified proteins aid in diagnosis of autoimmune hepatitis and associate with complete biochemical response to treatment

doi: 10.3389/fmed.2023.1195747

Figure Lengend Snippet: Characteristics of untreated AIH patients in the AILD cohort ( n = 58).

Article Snippet: We did not observe a significant difference in the presence of anti-PTM antibodies in patients positive or negative for ANA or SMA, with the exception of anti-MAA positivity and ANA positivity in patients with AIH (Chi-2 (1) > = 4.687, p = 0.030).

Techniques: Biomarker Discovery

Levels of (A) ALAT, ASAT, IgG and (B) anti-PTM antibodies over time in patients with AIH ( n = 25). ALAT, ASAT and IgG levels were determined as standard procedure after inclusion. V1: before commencing treatment, V2: during treatment. Median time interval: 65 months (6–138). Reactivity toward anti-PTM antibodies was determined using ELISA and is depicted as arbitrary units per milliliter (aU/mL). * p = 0.0244 and **** p ≤ 0.0001. AGE, advanced glycation end-product; AL, acetylated protein; ALAT, Alanine aminotransferase; ASAT, Aspartate aminotransferase; CarP, carbamylated protein; IgG, immunoglobulin gamma; MAA, malondialdehyde–acetaldehyde adduct; V1, first visit; V2, second visit.

Journal: Frontiers in Medicine

Article Title: Antibodies against multiple post-translationally modified proteins aid in diagnosis of autoimmune hepatitis and associate with complete biochemical response to treatment

doi: 10.3389/fmed.2023.1195747

Figure Lengend Snippet: Levels of (A) ALAT, ASAT, IgG and (B) anti-PTM antibodies over time in patients with AIH ( n = 25). ALAT, ASAT and IgG levels were determined as standard procedure after inclusion. V1: before commencing treatment, V2: during treatment. Median time interval: 65 months (6–138). Reactivity toward anti-PTM antibodies was determined using ELISA and is depicted as arbitrary units per milliliter (aU/mL). * p = 0.0244 and **** p ≤ 0.0001. AGE, advanced glycation end-product; AL, acetylated protein; ALAT, Alanine aminotransferase; ASAT, Aspartate aminotransferase; CarP, carbamylated protein; IgG, immunoglobulin gamma; MAA, malondialdehyde–acetaldehyde adduct; V1, first visit; V2, second visit.

Article Snippet: We did not observe a significant difference in the presence of anti-PTM antibodies in patients positive or negative for ANA or SMA, with the exception of anti-MAA positivity and ANA positivity in patients with AIH (Chi-2 (1) > = 4.687, p = 0.030).

Techniques: Enzyme-linked Immunosorbent Assay

A brief summary of studies addressing immune and autoimmune side effects of COVID-19 vaccines.

Journal: Frontiers in Immunology

Article Title: COVID-19 Vaccination and the Rate of Immune and Autoimmune Adverse Events Following Immunization: Insights From a Narrative Literature Review

doi: 10.3389/fimmu.2022.872683

Figure Lengend Snippet: A brief summary of studies addressing immune and autoimmune side effects of COVID-19 vaccines.

Article Snippet: , AstraZeneca (ChAdOx1) , Rela et al. ( ) , 2 cases of AIH following 1 st vaccination , There were no clear clinical or biochemical features apart from a chronological association to differentiate patients’ vaccine-related AIH from idiopathic AIH..

Techniques: Vaccines, Biomarker Discovery, Infection, Diagnostic Assay, Injection, Imaging, Plasmid Preparation, Clinical Proteomics, Variant Assay, Coagulation, Activity Assay, Sequencing, Produced, Activation Assay

Updated RUCAM for the hepatocellular injury of DILI and HILI RUCAM: Roussel Uclaf Causality Assessment Method scale; DILI: Drug-induced liver injury; HILI: Herb-induced liver injury (HILI) [ <xref ref-type= 17 ] * Group I (7 causes) HAV: Anti-HAV-IgM, Hepatobiliary sonography/color Doppler, HCV: Anti-HCV, HCV-RNA, HEV: Anti-HEV-IgM, anti-HEV-IgG, HEV-RNA, Hepatobiliary sonography/color Doppler sonography of liver vessels/ endo-sonography/CT/MRC, Alcoholism (AST/ALT ≥ 2), Acute recent hypotension history (particularly if underlying heart disease), *Group II (5 causes) Complications of underlying disease(s) such as sepsis, metastatic malignancy, autoimmune hepatitis, chronic hepatitis B or C, primary biliary cholangitis or sclerosing cholangitis, genetic liver diseases, Infection suggested by PCR and titer change for; CMV (anti-CMV-IgM, anti-CMV-IgG), EBV (anti-EBV-IgM, anti-EBV-IgG), HSV (anti-HSV-IgM, anti-HSV-IgG), VZV (anti-VZV-IgM, anti-VZV-IgG). **Patient's ALT 689 U/L, Upper limit of normal ALT 40 U/L, Patient's ALP 213 U/L, Upper limit of normal ALP 120 U/L, R-value 9.7, RUCAM score > 5. The hepatocellular pattern of liver injury. Recommend acute viral hepatitis serologies, HCV RNA and autoimmune hepatitis serologies, and imaging studies such as abdominal ultrasound) [ 18 ]." width="100%" height="100%">

Journal: Cureus

Article Title: COVID-19 Vaccination-Induced Cholangiopathy and Autoimmune Hepatitis: A Series of Two Cases

doi: 10.7759/cureus.30304

Figure Lengend Snippet: Updated RUCAM for the hepatocellular injury of DILI and HILI RUCAM: Roussel Uclaf Causality Assessment Method scale; DILI: Drug-induced liver injury; HILI: Herb-induced liver injury (HILI) [ 17 ] * Group I (7 causes) HAV: Anti-HAV-IgM, Hepatobiliary sonography/color Doppler, HCV: Anti-HCV, HCV-RNA, HEV: Anti-HEV-IgM, anti-HEV-IgG, HEV-RNA, Hepatobiliary sonography/color Doppler sonography of liver vessels/ endo-sonography/CT/MRC, Alcoholism (AST/ALT ≥ 2), Acute recent hypotension history (particularly if underlying heart disease), *Group II (5 causes) Complications of underlying disease(s) such as sepsis, metastatic malignancy, autoimmune hepatitis, chronic hepatitis B or C, primary biliary cholangitis or sclerosing cholangitis, genetic liver diseases, Infection suggested by PCR and titer change for; CMV (anti-CMV-IgM, anti-CMV-IgG), EBV (anti-EBV-IgM, anti-EBV-IgG), HSV (anti-HSV-IgM, anti-HSV-IgG), VZV (anti-VZV-IgM, anti-VZV-IgG). **Patient's ALT 689 U/L, Upper limit of normal ALT 40 U/L, Patient's ALP 213 U/L, Upper limit of normal ALP 120 U/L, R-value 9.7, RUCAM score > 5. The hepatocellular pattern of liver injury. Recommend acute viral hepatitis serologies, HCV RNA and autoimmune hepatitis serologies, and imaging studies such as abdominal ultrasound) [ 18 ].

Article Snippet: A recent mention of AIH post-BNT162b2 mRNA (Pfizer-BioNTech) COVID-19 vaccination has been published by Fimiano et al. [ ] who reported a patient with AIH post-COVID-19 vaccination and suggested an increase in prevalence, and hence a need for increased awareness of possible COVID-19 vaccine-induced AIH [ ].

Techniques: Infection, Imaging