Survival and digestibility of orally-administered immunoglobulin preparations containing IgG through the gastrointestinal tract in humans

Many of the first published clinical studies on the digestibility of orally-administered IgG were conducted in infant populations. Zinkernagel et al. [9] fed 10 healthy infants at less than three weeks of age a lyophilized bovine colostrum preparation containing 70% IgG administered at 2 g/kg/d. An average 13%-20% of the Ig survived undigested in the stool as demonstrated by an agglutination assay against E. coli antigens [9]. In addition, recovered titer correlated with the amount of undigested IgG. In another study, 6 healthy immature, formula-fed infants ingested a 10% human immune serum globulin (HISG), predominantly IgG, in divided doses of 1 to 8 ml/kg/day over 5 consecutive days [10]. The survival of IgG in stool over a 24 hour period ranged between 4-12% of the original IgG ingested. Variability per subject was observed in the survival of active IgG in feces; however, increasing doses were associated with higher amounts of IgG excreted per day. There was no evidence of systemic absorption or adverse events.

In a larger randomized, controlled clinical trial, low-birth weight infants unable to breast feed were administered 600 mg daily of serum-derived human IgA (73%) and IgG (26%). The test group (n = 91) ingested the serum-derived IgA-IgG mixed into either infant formula or infant formula combined with pooled, pasteurized human milk. The control group (n = 88) ingested the same formula/milk preparation, less the serum-derived IgA-IgG [11]. The infants receiving oral IgA-IgG had fewer cases of necrotizing colitis (0 cases) compared to the controls (6 cases) and had “substantial amounts” of intact IgA and IgG recovered in stool compared to the controls. As in the previous study, there was no evidence of systemic absorption.

Bovine milk Ig concentrate purified from hyperimmunized cows against four human rotavirus serotypes has also been studied in a group (n = 164) of low birth weight infants [12]. The infants were dosed at 2 g Ig concentrate/kg/day for five days. Of the infants receiving Ig, stool samples from 47% had detectable bovine IgG and 43% maintained rotavirus-neutralization activity against bovine rotavirus V1005, human rotavirus Wa (serotype 1) and simian rotavirus SA-11 in cell culture. Furthermore, the infants with high amounts of neutralizing activity still present in feces demonstrated clinical benefit [12].

One small (N = 3) and another larger study (N = 105) have been performed to assess recovery of active IgG against rotavirus from feces of children [13,14]. The smaller study was comprised of three pediatric patients ages 16 months and 4 yr, both with severe combined immunodeficiency disease, and 18-yr-old with common variable immunodeficiency disease [13]. All three had a history of intermittent positive excretion of rotavirus serotype 1 with chronic diarrhea, decreased weight gain and fat malabsorption. The children ingested a single dose of 150 mg/kg human sera Ig (IgG at 50 mg/ml) labeled with ¹²⁵I. Approximately 50% of the recovered radioactivity was excreted in the stools over a 3 d period. Half of the excreted radioactively labeled IgG, or 25% of the originally ingested IgG, retained immunological activity, as determined by the recovery of ¹²⁵I-labeled Ig bound to rotavirus [13].

In the second study, children drank 100 ml of whole cow’s milk supplemented with hyperimmunized bovine colostrum against rotavirus, 3 times daily for a period of 6 days [14]. There were five groups based on the rotavirus-antibody titer of the Ig formulation: control (no rotavirus antibody titer), 1:2,500, 1:5,100, 1:8,000, and 1:8,200. After pooling results from the four experimental groups, approximately 5% of IgG was recovered while the level of antibody activity varied considerably. Approximately 88% of the experimental patients had detectable neutralization signals which correlated (r = 0.81) with percent reduction of rotavirus from stools and the titer of ingested milk/colostrum.

Two studies in adults measured the ileal recovery of orally-administered Igs [4,6]. Healthy, fasted subjects (n = 7) drank 400 ml of a ¹⁵N-labeled bovine colostrum-derived Ig fraction, containing approximately ~5.2% IgG, 0.86% IgM, and 0.1% IgA (~2 g IgG, 0.34 g IgM, and 0.04 g IgA) and ileal effluents were collected every 20 min for 8 hrs [4]. Approximately 19% of IgG and IgM was still immunologically active from ileal effluent, although the titer was not reported. The authors also reported that 59% of IgG collected from 2 subjects in the jejunum remained active. Further purification of the ileal chyme samples using protein chromatography demonstrated that the fractions with the most immunological activity had a molecular weight of ~100 kDa (kilo-Dalton) which correlates well with in vitro pepsin and trypsin digestion experiments of the intact IgG (~160 kDa) into Fab_1,2 dimers (~100 kDa) and monomers (~50 kDa) [15]. Thus, in addition to demonstrating IgG survivability through the gastric environment into the ileum, these data establish that in vivo IgGs are digested in a step-wise manner into active, intact Fab fragment that still bind target antigen (s).

In the second ileal recovery study, 6 healthy volunteers with an end ileostomy ingested 5 g of bovine-Ig concentrate from hyperimmune bovine colostrum against C. difficile which contained 2.1 g of IgG alone, with an antacid, during treatment with omeprazole (a proton-pump inhibitor which decreases the acidity of the stomach), or within enteric-coated capsules in four separate experiments [6]. The difference in IgG recovered was not statistically significant: alone (49%), antacid (30%) and omeprazole (50%) (p = 0.13). Counterintuitively, enteric encapsulation resulted in statistically less IgG reaching the ileum (4%) during the time course, compared with both the alone and omeprazole group. Some capsules were recovered intact or partially digested, suggesting that enteric encapsulation inhibited release of IgG in the small intestine. Percent recovery of IgG correlated with neutralizing activity of toxin A. These two studies illustrate that a high percentage of orally-administered IgG (between ~19% and ~50%) can be recovered intact and active from the distal ileum in adult humans before entering the large intestine.

Fecal recovery of orally-administered Igs has also been demonstrated in healthy adults. In one study, healthy adult volunteers (n = 6) took a single oral dose of bovine Ig concentrate (BIC, 45 g with 14.2 g of IgG) from the colostrum of hyperimmunized cows against C. difficile [5]. Each subject had a 14-day wash-out period between crossing-over into one of six testing groups: fasting (45 g BIC), fed (45 g BIC), fed (8 g BIC), co-administered with antacid (45 g BIC), with omeprazole (45 g BIC), and enteric-coated capsules (8 g BIC) designed to release the product at pH > 6 in the intestinal tract. Total bovine IgG and specific anti-C. difficile IgG activity were measured in feces. The bovine IgG concentration of the fasting group compared to the ingested dose of 45 g BIC after 72 hr in feces was 3.8%, for fed 1.6%, and for antacid 2.7%. Omeprazole increased fecal bovine IgG levels to 8.8%, although not statistically significant over the other groups. In this study, the stool samples from enteric-coated capsules had 32.7% of the IgG in the original dose, 8 g BIC. For the fed group ingesting 8 g BIC, the recovery was 0.6% the original dose. C. difficile neutralizing activity correlated with the percentage of IgG recovered. This study showed that enteric encapsulation of oral Ig correlated with higher amounts of IgG recovered in stool and therefore delivered more intact IgG to the colon in healthy adults. Further studies are required to determine whether enteric encapsulation is necessary to protect orally delivered Ig for efficacy in specific intestinal disorders.

Tacket et al. [16] administered two specific preparations of bovine colostrum against Shigella flexneri 2a strain 5427 T liposaccharide, anti-LPS IgG which varied by titer of anti-LPS (1:2,560 and 1:40,960, respectively) and addition of chocolate dairy protein powder (1:40,960 titer only) to healthy adults (n = 50). The healthy adults were challenged with 10³c.f.u. of S. flexneri 2a strain 2457 T after three days of ingesting the Ig concentrates above. Bovine IgG was detected in feces at 91% (1:2,560) and 60% (1:40,960) of the original amounts. In both groups, the recovered titer of bovine anti-LPS was ≥ 1:8. This study illustrated a dose–response effect since the group with the higher titer was better protected from S. flexneri challenge. In another report of two trials, 2 g of bovine Ig concentrate from the colostrum of cows hyperimmunized against cholera toxin was administered to patients with active cholera diarrhea under different protocols: two doses (4 g bovine Ig concentrate, n = 45) or a single dose for every two hours for a total of eight doses (16 g of Ig concentrate, n = 20). From the 65 patients, a total of 35 individual stool samples were analyzed for bovine IgG and IgA. Low levels of active Ig, either as whole IgG or Fab fragments, was found in stool for roughly 60% of the patients ingesting bovine Ig. An average of about 10-20% cholera toxin neutralizing activity was still present in the recovered stools, although the titer was not reported [17]. In another randomized, controlled trial, patients undergoing bone marrow transplantation (N = 72) who received either 50 mg/kg human gammaglobulin or placebo daily in four divided doses for 28 days after the procedure (500 mg weekly), there was 1 to 80 mg/dL of IgG present in stool. Antibody reactivity was not reported [18].

Other trials reporting only trace amounts of IgG in feces have also been performed. In an unpublished study of 12 healthy adults, when 10 g of serum-derived bovine immunoglobulin/protein isolate (SBI) was given on two consecutive days followed by 2.5 g for 14 days, there were only low levels of detectable IgG in feces [Hanning, R. and M. Drew, Bovine Immunoglobulin Feeding Trial. Data on File, 1994]. There was no detectable bovine Ig in the serum of any subjects again supporting the notion of no intact systemic circulation of bovine-derived Ig. In another study, when 0.5, 2.5, or 10 g of bovine IgG was administered to 4 healthy adults, only 0.01% of the ingested IgG was detected in feces. Neutralizing activity of this recovered fraction was not assessed [19]. Similarly, when a 15 g colostrum preparation from non-immunized cows with an IgG concentration of 51% was given to healthy volunteers (n = 8), there was no evidence of systemic absorption of bovine IgG (blood or urine) and in 3 of the 8 patients there were only trace amounts of bovine IgG detected in feces, but without antibody reactivity to Yersinia enterocolitica and Campylobacter jejuni antigens [20]. These data suggest that the study population may be an important determinant in recovery Ig and neutralizing activity. In healthy individuals with normal transit times, there appears to be less recovery of orally administered Ig compared to patients with accelerated intestinal transit due to infection or disease.

Recovered IgG values varied from study to study. This is not surprising since each study had different patient populations and various immunoglobulin preparations. Yet, these data summarized above strongly suggest that IgG are more resistant to complete digestion throughout the human GI tract than other dietary proteins since only three of the fifteen reports illustrate trace amounts of IgG recovered. It should be mentioned that with respect to nutrition literature, the term “digestibility” is most recently defined as the net absorption of an amino acid [21]. In this review, we are using the term “digestibility” to discuss the integrity of the quaternary and tertiary structure of IgG as it passes through the GI tract in humans, as it is generally understood that IgG can only bind to antigens within the GI tract if the antigen binding domain, the Fab, is intact. This would mean the Fab domain must resist complete denaturation through acidic pH and complete digestion by proteolytic enzymes. Most of the human studies summarized above for IgG assessed crude protein digestibility because they reported a percentage of intact IgG recovered, either from the ileum or from feces. As aforementioned, the many nutrition experiments which assess the digestibility of other dietary proteins are reported as percentages as a function of the net absorption of an amino acid. Therefore, it is difficult to compare the digestibility of IgG as reported in this review (crude protein) to the digestibility of other dietary proteins reported in literature (ileal digestibility as absorbed amino acids). In order to provide some sort of comparable measure, the true ileal digestibility - as defined as absorbed amino acids - of other dietary proteins in humans are: 95% for milk proteins, 94.1% for casein, 90% for pea protein, 91.5% for wheat protein [22]. There is one study reviewed in this manuscript which could conservatively be compared to the above numbers. Roos et al. [4], reported a prececal nitrogen absorption from the Ig preparation to be at 79%, below the absorption percentages mentioned above for other dietary proteins. In addition, recovered active fragments corresponding to ~100 kDa or two Fab domains were purified from the recovered chyme. This study therefore directly corroborates the step-wise process by which IgG are digested by enzymes in vitro also occurs in humans in vivo and that Ig preparations are digested more slowly, corresponding to less amino acid absorption via nitrogen monitoring. There are biochemical in vitro experiments which have assessed if various structural features of IgG contribute to overall stability. It is useful to discuss such experiments insofar that the majority of clinical studies reviewed in this manuscript illustrate a percentage of IgG and the Fab domains retained neutralizing activity albeit at a reduced level and more importantly, that a percentage of IgG and Fab domains retain their structural integrity, remaining intact.

The protein melting temperature (T_M) is the point at which a protein unfolds, or denatures, and lacks the structure necessary for activity. T_M is a biochemical measurement to probe protein structure in different situations, such as pH. Thermal stability of an IgG correlates with pH: lower pH values, 2.8-3.4, corresponded to lower average global T_M values, 43.7°C-53.6°C, and higher pH, 5.0-7.5, corresponded to higher average global T_M values, 67.5°C-68°C [33]. Even in the acidic pH range of 2.8-3.4, the T_M value does not fall below body temperature, 37°C, accounting for Ig structural integrity in the digestive tract. The addition of sugars, trehalose [34] and sucrose [35] to experimental buffers increased T_M values for all IgGs with pH values ranging from 4.0-8.0 suggesting that other environmental factors within the GI tract, like dietary molecules, could increase Ig stability. Salt content does not appear to affect IgG stability [35]. There have been isolated reports where the CH2 domain, the most thermally stable domain of the IgG, exhibits increased thermal stability after exposure to pH of 2.0 [36]. This increased stability is correlated with alternate conformations that various IgGs exhibit at this low pH [37-39]. Some IgG purification procedures, either from recombinant expression methods used to produce commercially-available biologic drugs or from naturally occurring sources, such as serum, require acidic or basic exposure steps [40,41]. IgG molecules purified utilizing pH shifts do not lose their capacity to bind antigens. In fact, certain intravenous immunoglobulin (IVIg) preparations purified with a low-pH step have enhanced in vitro and in vivo binding to antigens that correlates with better performance in mouse models of sepsis [41-43]. These studies underscore that IgG remain stable in acidic conditions at body temperature. It is also possible that transient exposure to acidic conditions in the stomach may increase stability for survival down the GI tract and to proteolytic enzymes.

Characterization of IgG structure using in vitro digestion with proteolytic enzymes dates to the 1960s [44-47]. It is well-established that enzymatic digestion of IgG at the hinge region with papain produces two active domains, Fab_1,2 and Fc (Figure 1BC). Furthermore, modulating reaction time, pH and temperature during enzymatic digestion will result in a variety of active domain fragments [48]. The primary digestive enzymes in humans for proteins are pepsin, in the stomach, followed by trypsin and chymotrypsin, in the small intestine [49] which digest IgG to Fab dimers (~100 kDa) and monomer Fab fragments (~50 kDa) [15], but this enzymatic susceptibility may vary by IgG subtype and species. Bovine IgG₁, for example, is more readily proteolyzed by pepsin than bovine IgG₂ [50]. Bovine IgG is more stable to proteolytic digestion compared to rabbit or human IgG [29]. Even after proteolytic digestion of IgG, Fab dimers and monomer fragments retain binding and antigen-neutralizing activity as long as they are not denatured. Proteolytic characterization of bovine derived IgG₁in vitro demonstrates intact and reactive Fab domains [29,50-53]. This correlates with the human in vivo study by Roos et al. [4] demonstrating that immunologically active bovine Fabs were recovered in ileal aspirates.