What is the evidence for using EnteraGam to treat pathophysiologic GI conditions?

Comment by InpharmD Researcher

Evidence supporting the use of serum-derived bovine immunoglobulin/protein isolate (SBI; EnteraGam®) for pathophysiologic gastrointestinal conditions is limited. Available data consist primarily of narrative reviews, small-scale clinical studies, and case series evaluating conditions such as diarrhea-predominant irritable bowel syndrome (IBS-D), HIV-associated enteropathy, and refractory inflammatory bowel disease (Tables 1-7). These publications suggest that SBI may improve gastrointestinal symptoms, including diarrhea, stool consistency, abdominal pain, bloating, urgency, and, in some populations, markers of intestinal function and mucosal immunity in patients whose symptoms have persisted despite multiple prior lines of therapy. Proposed mechanisms for its efficacy include binding microbial and pro-inflammatory antigens, supporting intestinal barrier integrity, reducing intestinal permeability, and promoting immune homeostasis. However, the evidence is limited by small sample sizes and predominantly exploratory or noncomparative study designs, and current clinical practice guidelines do not include SBI among recommended therapies for IBS-D. Additional well-designed randomized controlled trials are needed to better define its efficacy and role in the management of pathophysiologic gastrointestinal conditions.

Background

A 2022 American Gastroenterological Association clinical practice guideline evaluated pharmacologic therapies for irritable bowel syndrome with diarrhea (IBS-D) using the Grading of Recommendations Assessment, Development and Evaluation framework. The guideline provides conditional recommendations for eluxadoline, rifaximin, alosetron, loperamide, tricyclic antidepressants, and antispasmodics, and a conditional recommendation against selective serotonin reuptake inhibitors; however, serum-derived bovine immunoglobulin/protein isolate (SBI; EnteraGam®) was not included among the reviewed or recommended therapies. Therefore, while this guideline provides relevant context regarding evidence-supported pharmacologic options for IBS-D, it does not directly provide evidence supporting the use of EnteraGam® for pathophysiologic gastrointestinal conditions. [1]

Multiple review articles have evaluated the potential role of SBI in gastrointestinal disorders characterized by impaired intestinal barrier function, inflammation, and chronic diarrhea. These publications suggest that SBI may provide nutritional support in conditions such as IBS-D and HIV-associated enteropathy through proposed mechanisms including binding and neutralizing microbial and pro-inflammatory antigens, supporting intestinal barrier integrity, promoting a more favorable gut microbiota, reducing gut permeability, and helping maintain immune homeostasis. While these reviews describe improvements in gastrointestinal symptoms and nutritional status reported in preliminary human studies and preclinical models, the evidence is largely derived from narrative reviews rather than randomized comparative clinical trials. [2], [3], [4], [5], [6]

Within IBS-D, a 2017 review described SBI as a potential adjunctive medical food that may be incorporated into individualized treatment plans alongside dietary interventions and pharmacologic therapies such as rifaximin and eluxadoline. The review emphasized that management should be tailored to symptom severity, psychosocial factors, and patient-specific needs because no standard treatment algorithm exists. SBI was presented as one component of a multimodal, patient-centered approach rather than a replacement for established therapies. [2], [3], [4], [5], [6]

A 2021 commentary proposed a theoretical role for SBI in COVID-19 based on the interaction between gastrointestinal health and systemic inflammation. The authors hypothesized that SARS-CoV-2 infection may increase intestinal permeability, alter the gut microbiome, and contribute to systemic inflammation and cytokine release. They suggested that SBI, a protein preparation composed of >90% protein containing approximately 50% IgG, 10% bovine serum albumin, 6% transferrin, and 5% combined IgA/IgM, could potentially mitigate these processes by binding inflammatory antigens, reducing intestinal permeability, improving the gut microbiome, and interfering with viral protein binding to ACE2 receptors. However, these proposed benefits were hypothesis-generating and based on biologic rationale and preclinical evidence rather than clinical efficacy studies in patients with COVID-19. [2], [3], [4], [5], [6]

Background References: [1] Lembo A, Sultan S, Chang L, Heidelbaugh JJ, Smalley W, Verne GN. AGA Clinical Practice Guideline on the Pharmacological Management of Irritable Bowel Syndrome With Diarrhea. Gastroenterology. 2022;163(1):137-151. doi:10.1053/j.gastro.2022.04.017
[2] Lucak S, Chang L, Halpert A, Harris LA. Current and emergent pharmacologic treatments for irritable bowel syndrome with diarrhea: evidence-based treatment in practice. Ther Adv Gastroenterol. 2017;10(2):253-275. doi:10.1177/1756283X16663396
[3] Petschow BW, Blikslager AT, Weaver EM, et al. Bovine immunoglobulin protein isolates for the nutritional management of enteropathy. World J Gastroenterol. 2014;20(33):11713-11726. doi:10.3748/wjg.v20.i33.11713
[4] Petschow BW, Burnett BP, Shaw AL, Weaver EM, Klein GL. Dietary requirement for serum-derived bovine immunoglobulins in the clinical management of patients with enteropathy. Dig Dis Sci. 2015;60(1):13-23. doi:10.1007/s10620-014-3322-0
[5] Utay NS, Asmuth DM, Gharakhanian S, Contreras M, Warner CD, Detzel CJ. Potential use of serum-derived bovine immunoglobulin/protein isolate for the management of COVID-19. Drug Dev Res. 2021;82(7):873-879. doi:10.1002/ddr.21841.
[6] Petschow BW, Burnett B, Shaw AL, Weaver EM, Klein GL. Serum-derived bovine immunoglobulin/protein isolate: postulated mechanism of action for management of enteropathy. Clin Exp Gastroenterol. 2014;7:181-190.
Literature Review

A search of the published medical literature revealed 7 studies investigating the researchable question:

What is the evidence for using EnteraGam to treat pathophysiologic GI conditions?

Level of evidence

C - Multiple studies with limitations or conflicting results  Read more→



Please see Tables 1-7 for your response.


Evaluation of Serum-Derived Bovine Immunoglobulin Protein Isolate in Subjects with Diarrhea-Predominant Irritable Bowel Syndrome
Design

Randomized, double-blind, placebo-controlled, pilot  study

N= 66

Objective To evaluate the impact of oral serum-derived bovine immunoglobulin/protein isolate (SBI) on gastrointestinal (GI) symptom scores and quality of life (QoL) in subjects with diarrhea-predominant irritable bowel syndrome (IBS-D)
Study Groups

SBI 10 g/day (n= 25)

SBI 5 g/day (n= 19)

Placebo (n= 22)

Inclusion Criteria Adults aged 18-65 years diagnosed with IBS-D at least 6 months prior to enrollment, experiencing symptoms according to ROME II criteria
Exclusion Criteria Constipation-predominant IBS, history of serious GI, hepatic, renal, cardiovascular, neurological, or hematological disorders, drug or alcohol abuse, psychiatric disorders, or allergy to study-related products
Methods

In a controlled study lasting 6 weeks, subjects were randomly assigned to one of 3 treatment groups after a one-week screening period. The groups were: a placebo group receiving 10 g/day soy protein isolate, an SBI 5 g/day plus 5 g/day placebo group, and an SBI 10 g/day group. The SBI 5 g/day group also consumed 5 g/day soy protein isolate to ensure uniform protein intake across all groups. The SBI was presented as a protein powder, containing over 50% immunoglobulin (IgG) and other serum proteins akin to those in colostrum and milk. Notably, SBI was free from lactose, casein, whey, gluten, and soy protein, though it contained trace amounts of sunflower lecithin. Treatment products were supplied by Entera Health, Inc., in matched capsules containing 500 mg of soy protein isolate, 250 mg SBI plus 250 mg soy protein isolate, or 500 mg SBI. Participants were directed to take five capsules four times daily. Patient removal from the study was based on adverse events, physician's clinical judgment, personal reasons, or protocol violations.

Duration 6 weeks
Outcome Measures

Primary: Change in number of days per week with symptoms

Secondary: Symptom severity scores, IBS-36 questionnaire scores

Baseline Characteristics  

10 g/day SBI

(n = 15)

5 g/day SBI

(n = 16)

Placebo

(n = 14)

Sex - Female (n, %) 10 (66.7%) 8 (50.0%) 10 (71.4%)
Age, Mean ± SD (years) 49.1 ± 10.5 44.9 ± 8.7 47.8 ± 10.4
Weight, Mean ± SD (kg) 77.9 ± 18.8 86.6 ± 24.9 79.0 ± 10.9
BMI, Mean ± SD (kg/m2) 27.9 ± 4.8 29.0 ± 9.2 29.7 ± 5.0
Results  

10 g/day SBI

(n = 15)

5 g/day SBI

(n = 15)

Placebo

(n = 13)

Any symptom - Change -1.60 ± 2.03, p= 0.009 -1.36 ± 1.78, p= 0.014 -0.67 ± 2.02, p= 0.276
Abdominal pain - Change -2.00 ± 2.51, p= 0.008 -0.36 ± 1.86, p= 0.486 -0.92 ± 2.35, p= 0.204
Flatulence - Change -2.33 ± 2.47, p= 0.003 -1.43 ± 2.28, p= 0.035 -0.17 ± 1.27, p= 0.658
Bloating - Change -1.27 ± 2.22, p= 0.044 -0.14 ± 2.66, p= 0.844 -0.42 ± 2.50, p= 0.576
Loose stool - Change -2.07 ± 2.71, p= 0.011 -0.79 ± 2.33, p= 0.229 0.17 ± 3.16, p= 0.858
Urgency - Change -1.47 ± 2.64, p= 0.050 0.36 ± 1.98, p= 0.513 -0.25 ± 2.45, p= 0.731
Adverse Events Four subjects withdrew due to nausea: 2 in the 10 g/day SBI group, 1 in the 5 g/day SBI group, and 1 in the placebo group. No serious adverse events reported. 
Study Author Conclusions Nutritional therapy with SBI with either 10 g/day or 5 g/day of SBI in 30 patients was well tolerated and resulted in significant improvements in symptom days and daily symptom scores in IBS-D patients. Further studies with larger sample sizes are needed to validate these findings. 
Critique The study demonstrated significant within-group improvements in symptoms with SBI treatment, but the small sample size and lack of power to detect between-group differences limit the generalizability of the findings. Additionally, the study was not sufficiently powered for statistical comparison between groups, and the short duration may not capture long-term effects. 
Table 1 References:
[7] Wilson D, Evans M, Weaver E, Shaw AL, Klein GL. Evaluation of serum-derived bovine immunoglobulin protein isolate in subjects with diarrhea-predominant irritable bowel syndrome. Clin Med Insights Gastroenterol. 2013;6:49-60. doi:10.4137/CGast.S13200.

 

Oral serum-derived bovine immunoglobulin improves duodenal immune reconstitution and absorption function in patients with HIV enteropathy
Design

Open-label trial with intensive 8-week phase of bovine serum immunoglobulin (SBI) 2.5 g twice daily with a 4-week washout period and an optional 9-month extension study

N= 8

Objective To examine the impact of serum-derived bovine immunoglobulin, an oral medical food known to neutralize bacterial antigen and reduce intestinal inflammation, on restoration of mucosal immunity and gastrointestinal function in individuals with HIV enteropathy
Study Groups All participants (N= 8)
Inclusion Criteria Participants with HIV enteropathy defined as chronic gastrointestinal symptoms including loose or watery stools and increased stool frequency (>3/day) despite no identifiable, reversible cause
Exclusion Criteria Not specified
Methods Participants received 2.5 g of SBI twice daily for 8 weeks followed by a 4-week washout phase. Upper endoscopy for tissue immunofluorescent antibody assay and disaccharide gut permeability/absorption studies were performed before and after 8 weeks of SBI. Blood was collected for markers of microbial translocation, inflammation, and collagen kinetics. A validated gastrointestinal questionnaire assessed changes in symptoms. 
Duration 8 weeks of treatment with a 4-week washout period and an optional 9-month extension study
Outcome Measures Primary: Improvement in gastrointestinal symptoms, increase in mucosal CD4+ lymphocyte densities, D-xylose absorption
Baseline Characteristics  

All participants

(N= 8)

Median age, years 44.5 (38.8-47.8)
Median peripheral blood CD4+ T-cell count 372 cells/mL (193-459 cells/mL)

Antiretroviral therapy (ART) regimen

Protease inhibitor-based

Non-nucleoside reverse transcriptase inhibitor (NNRTI)-based

Integrase inhibitor-based

 

4

3  

1

Viral load Undetectable

Race, n (%)

White

African-American

 

5 (62.5%)

3 (37.5%)

Results   Baseline Week 8 p-value
Bowel movements/day 5.8 (5.0-8.4) 2 (2-3.8) 0.008
Stool consistency [1-formed to 6-watery] 5.3 (5-6) 3 (2.2-3.8) 0.008
Gastrointestinal questionnaire score 17 (15.6-21.8) 8.0 (3.5-11.9) 0.008
D-xylose absorption, mg 33.8 (28.7-38.2) 40.9 (19.8-44.4) 0.19
CD3+/CD4+ lymphocytes, cells/mm2 213 (152-243) 322 (228-433) 0.016
Adverse Events The only adverse event reported was perceived constipation when stool frequency fell to once a day in two participants.
Study Author Conclusions SBI significantly increases intestinal mucosal CD4+ lymphocyte counts, improves duodenal function, and showed evidence of promoting intestinal repair in the setting of HIV enteropathy.
Critique The study demonstrated significant improvements in gastrointestinal symptoms and mucosal immunity, but the small sample size and open-label design limit the generalizability of the findings. The lack of a control group and potential placebo effect should be considered. Further studies with larger sample sizes and control groups are needed to confirm these findings.
Table 2 References:
[8] Asmuth DM, Ma ZM, Albanese A, et al. Oral serum-derived bovine immunoglobulin improves duodenal immune reconstitution and absorption function in patients with HIV enteropathy. AIDS. 2013;27(14):2207-2217. doi:10.1097/QAD.0b013e328362e54c
New therapeutic option for irritable bowel syndrome: Serum-derived bovine immunoglobulin
Design

Retrospective chart analysis

N= 14

Objective To investigate the use of oral serum-derived bovine immunoglobulin/protein isolate (SBI) in the management of differing forms of irritable bowel syndrome (IBS)
Study Groups

IBS-D (diarrhea-predominant, n= 7)

IBS-C (constipation-predominant, n= 2)

IBS-M (mixed, n= 2)

IBS-U (undefined, n= 3)

Inclusion Criteria Patients with IBS (IBS-D, IBS-C, IBS-M, IBS-U) receiving SBI as an addition to standard care
Exclusion Criteria Not specified
Methods SBI (5 g or 10 g daily dose) was added to the patient's current standard care. Patients were followed for several weeks to assess symptom improvement. Outcomes were determined through direct questioning regarding changes from prior visits. 
Duration Several weeks (specific duration varied per patient)
Outcome Measures

Primary: Improvement in IBS symptoms (stool consistency, frequency, abdominal pain, bloating, distention, incontinence)

Secondary: Resolution of symptoms in some patients

Baseline Characteristics  

IBS-D

(n= 7)

IBS-C

(n= 2)

IBS-M

(n= 2)

IBS-U

(n= 3)

Age range, years 24-87 22-55 33-66 50-82
Gender 4M/3F 0M/2F 0M/2F 1M/2F
Results  

IBS-D

(n= 7)

IBS-C

(n= 2)

IBS-M

(n= 2)

IBS-U

(n= 3)

Improvement in symptoms 7/7 1/2 2/2 2/3
Resolution of symptoms 2/7 0/2 0/2 2/3
Adverse Events No adverse effects were noted due to SBI therapy in any of the IBS patient populations. 
Study Author Conclusions SBI is effective in managing IBS-D symptoms and shows potential for other IBS forms. It provides a safe option for IBS management, particularly for IBS-D, and further investigation is needed for other IBS types. 
Critique The study is limited by its small sample size and retrospective design. While promising results were observed, particularly for IBS-D, the findings may not be generalizable. Further research with larger sample sizes and controlled designs is needed to confirm these results. 
Table 3 References:
[9] Good L, Rosario R, Panas R. New therapeutic option for irritable bowel syndrome: serum-derived bovine immunoglobulin. World J Gastroenterol. 2015;21(11):3361-3366. doi:10.3748/wjg.v21.i11.3361

Evaluation of oral serum-derived bovine immunoglobulins in HIV-infected patients with chronic idiopathic diarrhea
Design

Prospective, multi-center study with a partial cross-over design

N= 103

Objective To evaluate serum-derived bovine immunoglobulin/protein isolate (SBI) for safety and impact on gastrointestinal (GI) symptoms in HIV patients with chronic idiopathic diarrhea
Study Groups

Placebo BID (n= 36)

SBI 2.5 g BID (n= 34)

SBI 5 g BID (n= 33)

Inclusion Criteria Adult HIV-infected male or non-pregnant female patients who were virologically suppressed on anti-retroviral therapy (ART) for at least 12 months prior to screening and reported a history of chronic idiopathic diarrhea (defined as three or more unformed stools per day for at least 3 months)
Exclusion Criteria Positive stool test for pathogenic bacteria, ova or parasites during the 14-day screening period; changes in ART regimen during the 3-month period prior to screening; history of a condition that required chronic therapy that might alter the gut flora or use of an antibiotic within 2 weeks prior to screening; significantly abnormal lab results for alkaline phosphatase, aspartate aminotransferase (AST), alanine aminotransferase (ALT), and total bilirubin; patients not on stable ART regimen for at least 1 year and not virologically suppressed; active or history of GI disorders or pancreatitis; pregnancy; history of drug or alcohol abuse
Methods

This study included a double-blind, placebo-controlled  (PBO) lead-in phase followed by a 20-week, open-label, placebo-free dose-ranging extension phase.

Participants were randomized to receive placebo or SBI at 2.5 or 5.0 g BID for 4 weeks, followed by either a (1) 20-week, placebo-free phase with SBI at 2.5 g or 5.0 g BID or a (2) 24-week, placebo-free phase with SBI at 2.5 g or 5.0 g BID. Safety was evaluated by monitoring adverse events and clinical laboratory testing. Health status and changes in GI symptoms were assessed using validated questionnaires.

Duration April 2013 to March 2014
Outcome Measures

Primary: Change in the number of daily unformed stools

Secondary: Change in other daily GI symptom scores

Baseline Characteristics  

Placebo BID

(n= 36)

SBI 2.5 g BID

(n= 34)

SBI 5.0 g BID

(n= 33)

Total

(N= 103)

Male, n (%) 28 (78%) 21 (62%) 22 (67%) 71 (69%)
African-American, n (%) 21 (58%) 20 (59%) 22 (67%) 63 (61%)
White, n (%) 14 (39%) 14 (41%) 10 (30%) 38 (37%)
Age, years (range) 50 (34–66) 49 (34–70) 48 (32–65) 50 (32–70)
Time since HIV diagnosis, years (range) 16.7 (1.8–27.5) 16.4 (6.3–29.5) 19.2 (4.8–28.5) 18.2 (1.8–29.5)
Peripheral CD4+ T-cell count, cells/μL (range) 523 (194–1224) 813 (189–1611) 672 (202–1754) 637 (189–1754)
Plasma viral load, copies/mL (range) 19 (19–64) 19 (19–119) 19 (19–168) 19 (19–168)
Time on ART, years (range) 7.46 (1.0–23.07) 9.05 (1.0–23.67) 9.89 (1.0–23.73) 8.33 (1.0–23.73)
Time with HIV-associated Diarrhea, years (range) 2.2 (0.2–23.7) 4.7 (0.2–29.5) 5.5 (0.1–23.5) 3.5 (0.1–29.5)
Results  

PBO

(n= 36)

SBI 2.5 g

(n= 34)

SBI 5.0 g

(n= 33)

p-value
Stool consistency 4.9 ± 0.7 4.9 ± 0.7 5.0 ± 0.7 0.0001
Abdominal pain or discomfort 1.8 ± 0.9 1.6 ± 0.8 1.6 ± 0.8 0.0001
Urgency 0.7 ± 0.4 0.6 ± 0.4 0.6 ± 0.4 0.0001
Fecal incontinence 0.4 ± 0.4 0.2 ± 0.3 0.4 ± 0.4 0.0001
Nocturnal bowel movements 0.3 ± 0.4 0.3 ± 0.4 0.4 ± 0.4 0.018
Adverse Events SBI was well tolerated with only 2 withdrawals due to adverse events potentially associated with SBI. Common adverse events included flatulence, dyspepsia, nausea, constipation, and headache. No serious adverse events were reported during the PBO-controlled phase
Study Author Conclusions Oral SBI is safe and well tolerated at the doses studied in HIV patients with chronic diarrhea. No conclusions could be drawn regarding impact on GI symptoms. Additional studies are ongoing to examine the biological and immunologic effects of SBI in virologically suppressed HIV-infected patients.
Critique The study demonstrated the safety of SBI in HIV-infected patients, but the strong placebo effect and lack of significant differences between the placebo and SBI groups limit conclusions about efficacy. The study's design and the potential for recall bias in symptom reporting may have influenced the results. Further research is needed to explore the biological effects of SBI and its impact on GI symptoms in this population.
Table 4 References:
[10] Asmuth DM, Hinkle JE, LaMarca A, et al. Evaluation of oral serum-derived bovine immunoglobulins in HIV-infected patients with chronic idiopathic diarrhea. HIV Clin Trials. 2017 Nov-Dec;18(5-6):205-213. doi:10.1080/15284336.2017.1401256

 

Serum-derived bovine immunoglobulin for children with diarrhea-predominant irritable bowel syndrome
Design

Randomized, double-blind, placebo-controlled, pilot study

N= 15

Objective To determine if serum-derived bovine immunoglobulin (SBI) can improve symptoms in children with diarrhea-predominant irritable bowel syndromediarrhea-predominant irritable bowel syndrome (d-IBS)
Study Groups

SBI (n= 9)

Placebo (n= 6)

Inclusion Criteria Male and/or nonpregnant females between 8 and 18 years at the time of consent, newly diagnosed with d-IBS according to ROME III criteria
Exclusion Criteria Concurrent pharmacologic treatment for d-IBS, non-English speaker, known allergy or hypersensitivity to beef or any component of SBI, and pregnancy
Methods Patients were randomized to 5 g BID SBI or placebo for 3 weeks. 
Duration 3 weeks
Outcome Measures

Primary: Change in number of stools per week

Secondary: Changes in abdominal pain, stool consistency

Baseline Characteristics   SBI (n= 9) Placebo (n= 6)
Age, years 14.3 ± 3.7 12 ± 3.3
Male 4 of 9 2 of 6
Results   SBI Placebo

Number of stools per week

Screening week

End of treatment (week 3)

p-Value from week 1 to 3

 

18 ± 5.3

13.6 ± 5.4

0.07

 

19.7 ± 8.3

15.5 ± 13.6

0.12

Abdominal pain (Likert scale: 0= no pain, 4= severe pain)

Screening week

End of treatment (week 3)

p-Value from week 1 to 3

 

2.4 ± 0.6

1.7 ± 0.9

0.02

 

2.1 ± 0.7

1.6 ± 0.7

0.08

Stool form (Bristol stool scale: 1-7)

Screening week

End of treatment (week 3)

p-Value from week 1 to 3

 

5.3 ± 0.8

4.2 ± 1.2

0.05

 

5.1 ± 0.6

4.2 ± 2

0.28

Adverse Events No serious adverse events occurred. Serum chemistries and hemograms were normal at baseline and at the end of study in all patients.
Study Author Conclusions In this single-center, exploratory pilot study, we demonstrated that 10 g SBI per day was safe in children with d-IBS and improved symptoms. Larger studies, with longer treatment duration, seem warranted based on these initial positive results. 
Critique The study was underpowered with a small sample size, which may limit the generalizability of the findings. The short duration of 3 weeks may not be sufficient to observe long-term effects. The study population had a higher stool frequency than typical d-IBS patients, which may have influenced the results. Despite these limitations, the study provides initial evidence supporting the safety and potential efficacy of SBI in children with d-IBS. 
Table 5 References:
[11] Arrouk R, Herdes RE, Karpinski AC, Hyman PE. Serum-derived bovine immunoglobulin for children with diarrhea-predominant irritable bowel syndrome. Pediatr Health Med Ther. 2018;9:129-133. doi:10.2147/PHMT.S159925

Management of inflammatory bowel disease with oral serum-derived bovine immunoglobulin
Design

Single-center, retrospective, cohort study

N= 45

Objective To report the clinical effect of oral serum-derived bovine immunoglobulin/protein isolate (SBI) on symptom and disease management in patients with inflammatory bowel disease (IBD)
Study Groups

Crohn’s disease (CD, n= 38)

Ulcerative colitis (UC, n= 7)

Inclusion Criteria Patients diagnosed with IBD from a single gastroenterology practice near Orlando, FL, who had not responded to traditional pharmaceutical interventions in combination (i.e., tumor necrosis factor alpha agents, anti-inflammatory agents, immunomodulators)
Exclusion Criteria Not specified
Methods Patients were provided SBI (5 g/day, as EnteraGam®) for nutritional support in addition to their current therapy regimens for nutritional support. Symptom management was assessed at least monthly via phone using a Likert scale (ranging from 0= none to 4= complete). Patients were also asked about SBI compliance and side effects on a monthly basis. ANOVA and multivariate ordered logistical regression were used to analyze response to therapy based on patient characteristics and IBD diagnosis.
Duration 12 weeks (any patient with <12 weeks of SBI use had their last observation carried forward)
Outcome Measures

Primary: Clinical improvement in symptom scores

Secondary: Overall group response and percent improvement to SBI over 12 weeks

Baseline Characteristics  

Patients

(N = 45)

Male, n (%) 28 (62.2%)
White, n (%) 41 (91.1%)
Age, years 51.5 ± 19.0
Senior age group (⩾65 years), n (%) 10 (22.2%)

Inflammatory bowel disease

CD, n (%)

UC, n (%)

 

38 (84.4%)

7 (15.6%)

Results  

Odds ratio (95% CI)

Retrospective endpoint (week 12) vs baseline (week 1)

2.8 (1.266–6.016), p= 0.011

Response at week 12, female vs male 

1.2 (0.547–2.774)

Response at week 12, Non-Caucasian vs Caucasian

0.3 (0.057–1.487)

Response at week 12, age ⩾65 years vs age <65 years

1.1 (0.421–2.924)

Diagnosis of CD vs UC

0.3 (0.108–1.108)

Adverse Events No patient-reported side effects
Study Author Conclusions SBI improves clinical management of IBD patients who are not fully managed on traditional therapies and should be considered for nutritional support regardless of disease activity, location, phenotype, duration, or complexity.
Critique The study's retrospective design and small sample size limit the generalizability of the findings. The lack of a control group and reliance on patient-reported outcomes without endoscopic validation are significant limitations. A larger, controlled study is recommended to confirm these findings. Additionally, although included patients remained symptomatic despite prior pharmacologic combination therapy, patients were able to continue their other nutritional support regimens while receiving SBI, and the effects of these other therapies (with possible confounding) was not assessed in the study.
Table 6 References:
[12] Shafran I, Burgunder P, Wei D, et al. Management of inflammatory bowel disease with oral serum-derived bovine immunoglobulin. Ther Adv Gastroenterol. 2015 Nov;8(6):331-9. doi:10.1177/1756283X15593693

 

Clinical Efficacy of Serum-Derived Bovine Immunoglobulin in Patients with Refractory Inflammatory Bowel Disease
Design

Retrospective analysis

N= 12

Objective To evaluate the effectiveness of serum-derived bovine immunoglobulin (SBI) in the management of refractory inflammatory bowel disease (IBD), particularly symptoms of chronic diarrhea and loose stools
Study Groups All patients (n= 12)
Inclusion Criteria Patients with refractory IBD symptoms who continued to have diarrhea despite taking standard IBD therapies and received oral SBI 5 gram daily for at least 6 weeks
Exclusion Criteria Patients not compliant with daily SBI consumption for at least 6 weeks or could not be reached by phone
Methods Retrospective chart analysis of patients diagnosed with IBD who were refractory to standard treatment. Patients received oral SBI 5 gram daily for at least 6 weeks. Symptom severity and frequency were graded before starting SBI and at 6 weeks using a standardized patient assessment form. Means and standard deviations for all symptom scores at baseline and week 6 were analyzed. 
Duration 6 weeks
Outcome Measures Changes in severity, frequency, and mean symptom scores of nausea, vomiting, and diarrhea
Baseline Characteristics  

All patients

(N= 12)

Age, mean/range (years) 42/21-69
Female, n (%) 4 (33%)
Caucasian, n (%) 9 (75%)
African-American, n (%) 1 (8.33%)
Other races, n (%) 2 (16.66%)
5-aminosalicyclic acid use, n (%) 9 (75%)
Immunosuppressant use, n (%) 9 (75%)
Biologic agent use, n (%) 11 (91.66%)
Results  

At baseline 

(mean)

At 6 weeks 

(mean)

p-value

Vomiting

Severity

Frequency

Mean symptom score

 

0.25

0.25

0.25

 

0.16

0.16

0.16

 

0.33

0.33

0.33

Nausea

Severity

Frequency

Mean symptom score

 

1.83

1.66

1.75

 

1.33

1.25

1.29

 

0.02

0.13

0.03

Diarrhea

Severity

Frequency

Mean symptom score

 

3.66

3.83

3.75

 

2.75

2.75

2.75

 

0.0006

0.0001

0.0001

Abdominal pain

Severity

Frequency

Mean symptom score

 

1.83

2.16

2

 

1.91

2

1.95

 

0.67

0.61

0.87

Adverse Events No adverse side effects of SBI were reported in the study.
Study Author Conclusions Therapy with SBI alleviated some refractory gastrointestinal symptoms in patients with IBD, including nausea and diarrhea. Increased duration, dosage and/or frequency of SBI might provide additional symptom improvement and could be tested through controlled clinical trials with larger sample sizes and longer follow up.
Critique The retrospective design, lack of control group, and potential for recall bias are limitations. The study was limited by a small sample size and short duration of treatment. Compliance and follow-up were poor, which limited the ability to obtain treatment response information from more patients. Despite these limitations, the study adds to the growing volume of literature demonstrating the benefits of SBI in the presence of GI inflammation.
Table 7 References:
[13] Liaquat H, Ashat M, Stocker A, et al. Clinical Efficacy of Serum-Derived Bovine Immunoglobulin in Patients With Refractory Inflammatory Bowel Disease. Am J Med Sci. 2018;356(6):531-536. doi:10.1016/j.amjms.2018.08.019