Recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) is usually administered by injection, and its oral administration in a clinical setting has been not yet reported. Here we demonstrate the bioavailability of orally administered rhGM-CSF in healthy volunteers. The rhGM-CSF was expressed in Bombyx mori expression system (BmrhGM-CSF).
Methods and Findings
Using a single-dose, randomized, open-label, two-period crossover clinical trial design, 19 healthy volunteers were orally administered with BmrhGM-CSF (8 µg/kg) and subcutaneously injected with rhGM-CSF (3.75 µg/kg) respectively. Serum samples were drawn at 0.0h, 0.5h ,0.75h,1.0h,1.5h,2.0h ,3.0h,4.0h,5.0h,6.0h,8.0h,10.0h and 12.0h after administrations. The hGM-CSF serum concentrations were determined by ELISA. The AUC was calculated using the trapezoid method. The relative bioavailability of BmrhGM-CSF was determined according to the AUC ratio of both orally administered and subcutaneously injected rhGM-CSF. Three volunteers were randomly selected from 15 orally administrated subjects with ELISA detectable values. Their serum samples at the 0.0h, 1.0h, 2.0h, 3.0h and 4.0h after the administrations were analyzed by Q-Trap MS/MS TOF. The different peaks were revealed by the spectrogram profile comparison of the 1.0h, 2.0h, 3.0h and 4.0h samples with that of the 0.0h sample, and further analyzed using both Enhanced Product Ion (EPI) scanning and Peptide Mass Fingerprinting Analysis. The rhGM-CSF was detected in the serum samples from 15 of 19 volunteers administrated with BmrhGM-CSF. Its bioavailability was observed at an average of 1.0%, with the highest of 3.1%. The rhGM-CSF peptide sequences in the serum samples were detected by MS analysis, and their sizes ranging from 2,039 to 7,336 Da.
The results demonstrated that the oral administered BmrhGM-CSF was absorbed into the blood. This study provides an approach for an oral administration of rhGM-CSF protein in clinical settings.
Citation: Zhang W, Lv Z, Nie Z, Chen G, Chen J, Sheng Q, et al. (2009) Bioavailability of Orally Administered rhGM-CSF: A Single-Dose, Randomized, Open-Label, Two-Period Crossover Trial. PLoS ONE 4(5): e5353. https://doi.org/10.1371/journal.pone.0005353
Editor: Joseph Alan Bauer, Bauer Research Foundation, United States of America
Received: November 22, 2008; Accepted: March 29, 2009; Published: May 12, 2009
Copyright: © 2009 Zhang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The clinical trial was mainly funded by Zhejiang Chinagene Biopharmaceutical Co., Ltd. This work was also supported by the grants from the National High Technology Research and Development Program (No. 2007AA021703, No. 2007AA100504), the National Basic Research Program of China (No. 2005CB121006), the Zhejiang Natural Science Foundation (No. Y305171), and the National Natural Science Foundation of China (No.30740015). Zhejiang Chinagene Biopharmaceutical Co., Ltd also participated in the work (some aspects of the study, including enrolling participants and supervising clinical work, were carried out by the company-employed author). The other funding agents had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The investigational product ( BmrhGM-CSF capsule ) was donated by Zhejiang Chinagene Biopharmaceutical Co., Ltd. GGC, the director of R&D Department of Zhejiang Chinagene Biopharmaceutical Co., Ltd., supported this work. The other authors declare no competing interests exist.
Recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) acts on precursor cell proliferation in bone marrow. It also stimulates granulocytes, monocytes, and colony formation; and induces hyperplasy of macrophages  . This protein is primarily used in bone marrow transplantation, tumor chemotherapy, and the treatment of aplastic anemia and agranulocytosis related to AIDS –. The rhGM-CSF is an acidoglycoprotein containing 127 amino acid residues and has a molecular weight of 14.4 kDa to 32 kDa . It can be expressed in Escherichia coli, yeast, and mammalian cells , . Currently, the rhGM-CSF is administered by injection in clinical settings.
We expressed hGM-CSF in silkworm pupae bioreactor named as BmrhGM-CSF. It was purified and determined to have molecular weigh of 29 kDa , , . It's post-translational modifications were characterized in addition to its glycosylation , , ., The oral formulation of BmrhGM-CSF was used in our previous animal study. The results from preclinical studies demonstrated that orally administered BmrhGM-CSF could function as an active cytokine . The orally administered BmrhGM-CSF was shown to be absorbed into blood of mice, beagles, and macaques, which increased leukocyte counts. (1) In hematogenesis-inhibited mice, orally administered BmrhGM-CSF stimulated the colony formation in hemopoietic tissues on the spleen surface and DNA synthesis in the bone marrow. The effect was similar to that of injected Leucomax. (2) Hematogenesis-inhibited beagles treated with 60Co and orally administered BmrhGM-CSF had white blood cell counts reached 50% of their baseline values by 9th day, and recovered to the normal levels by 12th day. Moreover, the percentage of new granulocytes and promyelocytes in the bone marrow increased significantly. (3) The oral administration of BmrhGM-CSF to cyclophosphamide-treated macaques increased leukocyte production in a manner similar to that of Leucomax injections .
BmrhGM-CSF also promoted the production of granulocytes in macaques and beagles, and increased leukocyte counts in a dose-dependent manner. Western blotting analysis indicated that BmrhGM-CSF could be absorbed into blood through the intestinal parva .
The results from preclinical animal stuies have proven that BmrhGM-CSF could penetrate into the blood as an active cytokine through the oral administration . In this paper, we report the results of the bioavailability of the orally administered BmrhGM-CSF in a clinical trial.
A total of 22 male volunteers were screened for inclusion at 2nd Affiliated Hospital of Zhejiang University, School of Medicine (Hangzhou, China). Participants were considered eligible if they met the following criteria:
- apparently healthy;
- 18–40 years of age;
- no liver, kidney, gastrointestinal and metabolic disorders, or neuropsychiatric diseases;
- no medical history, drug allergies history or smoking or alcoholic drinking;
- 18 kg/m2≤BMI≤25 kg/m2;
- with good communication between researchers, to comply with the requirements of the entire study and
- with signed informed consent and conducted a comprehensive history and physical examination and laboratory tests including blood pressure, heart rate and body temperature measurements, blood examination, urine analysis, blood biochemistry and ECG, etc.
Exclusion criteria were:
- participating in other clinical trials in last 2 weeks;
- donating blood during the trial period or within last 1 month;
- not accepting physical examination;
- drug allergy or a history of allergic disease;
- history of drug abuse and
- with any chronic or acute disease.
The test and reference formulations
The test formulation was the BmrhGM-CSF capsule for the oral administration provided by Zhejiang Chinagene Biopharmaceutical Co., Ltd. Each capsule contained 60 µg of BmrhGM-CSF. The reference formulation was the rhGM-CSF for subcutaneous injection (150 µg/bottle) purchased from Guangzhou Baidi Biotechnology Co., Ltd .The rhGM-CSF for subcutaneous injection was expressed in E. coli. The subcutaneous injection site was at upper arm deltoid. Both the test and reference formulations were stored at 4°C.
Phase I trial was registered with http://www.chictr.org (ChiCTR-TRC-00000107). We conducted the study in accordance with good clinical practice guidelines, provisions of the Declaration of Helsinki, and regulations of the People's Republic of China. The protocol and consent forms were approved by the ethics committee of 2nd Affiliated Hospital of Zhejiang University, School of Medicine. The Data and Safety Monitoring Board monitored adverse events and confirmed the end points of the experiments if investigators observed adverse events. The written informed consent was obtained from all volunteers.
In a single-dose, randomized, open-label, two-period crossover clinical trial, 20 volunteers were divided into two groups, 10 for each. These groups were designated TR (Test Formulation/Reference Formulation) and RT (Reference Formulation/Test Formulation), respectively. Of which, 10 volunteers in the TR group was orally administered with BmrhGM-CSF (8 µg/kg) on Day 1. After a 7-day washout period, the subcutaneous injection of the reference formulation, rhGM-CSF (3.75 µg/kg) was given to each subject of the same TR group on Day 9. The same protocol was performed, vice versa, for the RT group as described in the participant flow chart (Figure 1). After fasting overnight for at least 10 h till 8:00 am on the following day, the subjects designated for the oral administration were given BmrhGM-CSF with 200 ml warm boiled water. The subjects designated for the subcutaneous injection were given the injection at the upper arm deltoid with rhGM-CSF. Followed by a 4-h period, all of the volunteers in both groups had the same low-fat meal. During the trial study, the subjects did not smoke or drink alcohol, caffeine-containing beverage, or fruit juice in order to avoid any possible interference on the absorption and metabolism of the drug. The administration order for the subjects depended on random drawn numbers. The administration intervals between subjects depended on the length of time required for withdrawing blood samples for 2 to 3 min.
The primary goals of the study were to: (1) investigate the bioavailability of orally administered BmrhGM-CSF in healthy volunteers; (2) demonstrate the presence of rhGM-CSF peptides in serum of volunteers orally administered with BmrhGM-CSF.
The hGM-CSF concentrations in the blood serum.
Blood (2 ml) was collected from the brachial vein with a single-use syringe after drug administration at 0.0h, 0.5h, 0.75h, 1.0h, 1.5h, 2.0h, 3.0h, 4.0h, 5.0h, 6.0h, 8.0h, 10.0h and 12.0h. The blood samples were drawn into EDTA-coated anticoagulation tubes, mixed thoroughly, and centrifuged at 3000 rpm. Then serum samples were collected and stored at 4°C for use. The hGM-CSF concentrations in the sera were determined by ELISA within 12h after collection. Human GM-CSF ELISA kits were purchased from Jingmei Bioengineering Co., Ltd (Beijing, China). In order to reduce pilot error, these human GM-CSF ELISA kits used were the same lot. The tests were performed according to the instruction of the ELISA kit. Briefly, a standard curve was generated as follows: a solution containing 2000 ng/L of hGM-CSF was prepared, and standard curve calibrators containing 7.8, 15.6, 31.2, 62.5, 125.0, 250.0, 500.0, and 1000.0 ng/L of hGM-CSF were generated by a serial dilution. The OD values of the standard curve calibrators, quality controls and samples tested were determined at a wavelength of 450 nm. The hGM-CSF concentrations of the tested samples were measured by the regression analysis with the CVXPT32 software.
The serum samples collected from 3 volunteers at the 0.0h, 1.0h, 2.0h, 3.0h , 4.0h after the oral administration of BmrhGM-CSF and the subcutaneous injection of rhGM-CSF were subjected to MS analysis (Q-Trap MS/MS TOF, ABI Co.) . Those 3 were randomly selected from 15 ELISA detectable subjects. The serum samples were diluted by 100-fold with 80% acetonitrile and the solution was centrifuged at 12,000 rpm for 10 min. The supernatant was collected for MS analysis. The 0.0h sample analysis spectrogram was used as control and compared with the analysis spectrogram of 1.0h, 2.0h, 3.0h and 4.0h hour sample in order to obtain peaks with different mass-to-electric charge ratios. Further analysis of the peaks through both Enhanced Product Ion (EPI) scanning and Peptide Mass Fingerprinting Analysis concluded that the molecular weight and amino acid sequences of these peptides matching hGM-CSF fragments.
In a single-dose, randomized, open-label, two-period crossover clinical trial, 20 enrolled participants were randomly assigned to two groups (TR and RT) in a 1∶1 ratio. Briefly, a randomization code was developed using a computer-generated randomization schedule (Compaq Visual Fortran version 6.5, IMSL Fortran Library, Compaq Computer Corp., Houston, Texas) by a biostatistician. After preparing a random sequence, subjects were allocated to the two trial groups by a physician who was not involved in the main research. During the process of allocation, each subject was given a unique identification code (Unique Identifier, UI). This UI was used as a label to uniquely identify the subject's group after completion of the study. During the study period this UI was given to the main researchers together with the necessary treatment for each participant. Both test and reference formulations of the rhGM-CSF were designed for either oral or subcutaneous administration in both RT and TR groups. Specifically, the test formulation of BmrhGM-CSF was orally administered to the TR group on Day 1. After a 7-day washout period, the reference formulation of rhGM-CSF was subcutaneously injected on Day 9. Conversely, for the RT group, the reference formulation of rhGM-CSF was subcutaneously injected on Day 1. After a 7-day washout period, the test formulation of BmrhGM-CSF was orally administered on Day 9.
The bioavailability was defined in accordance with the in vivo bioequivalence guidance criteria established by the US Food and Drug Administration . That states it is the rate and extent to which the active ingredient or active moiety is absorbed from a drug product and becomes available at the site of action of the formulations tested. An analysis of variance (ANOVA) for a 2×2 crossover design in ln-transformed Cmax, AUC0∼12 and AUC0∼∞ was performed to determine the bioavailability. The 90% CIs for the corresponding differences in Cmax, AUC0∼12 and AUC0∼∞ were calculated. ANOVA was performed using the F ratio. The probability (P) of exceeding the limits of acceptance (80%–125%) was obtained by two 1-sided t tests described by Schuirmann  . The 2 drug formulations were considered bioequivalent if the geometric mean ratios of the Cmax and AUC were within the predetermined range of 80% to 125% and if P for the 90% CIs was <0.05 . Statistical analysis of the drug product pharmacokinetics was carried out using WinNonlin version 5 (Pharsight Corporation, Mountain View, California).
Originally 22 healthy male volunteers were assessed for eligibility from September, 2005 to January, 2006 in Hangzhou City, Zhejiang Province. Two of them were subsequently excluded because they did not meet the inclusion criteria. The twenty volunteers were randomly divided into the TR and RT groups. One of them withdrew the consent resulting in 19 volunteers being analyzed for the primary outcome (Figure 1).
The blood hGM-CSF concentrations of 19 volunteers were determined by ELISA before and after the oral administration of BmrhGM-CSF. Of which, 15 showed significant detectable amount but 4. Figure 2 shows the time course of the average rhGM-CSF serum concentration of 19 subjects who received a single dose of either test BmrhGM-CSF or reference rhGM-CSF. Two hours after the oral administration of BmrhGM-CSF, its absorption peak increased to the amount of 40.1 ng/L. It then returned to the baseline level over the next 10 h.
A: Average hGM-CSF serum concentration versus time in 19 subjects after oral administration of BmrhGM-CSF (8 µg/kg). B: Average hGM-CSF serum concentration versus time in 19 subjects after subcutaneous injection of rhGM-CSF(3.75 µg/kg).
The values of the hGM-CSF in the sera and time points were fitted using the DASVer 2.0 software. The pharmacokinetics of each of the components was consistent with the two-compartment model. The area under the curve (AUC), Cmax, and Tmax for the test and reference formulations were calculated using the statistical moment method, and the related pharmacokinetic parameters are shown in Table 1.
The AUC was calculated using the trapezoid method. The AUC ratio of the test formulation to the reference formulation demonstrated an average bioavailability of the rhGM-CSF in the 19 subjects was 0.61% after oral administration. However, 4 of them showed an undetectable serum concentration of the rhGM-CSF resulting in their AUCs could not be calculated. If these subjects were excluded from the statistic analysis, thus the average bioavailability of the other 15 subjects could reach 1.0%; one of them showed the highest bioavailability of 3.1%.
Based on the bioavailability data analyses above, the serum samples from three of 15 subjects were used for the MS analyses. Those samples were randomly selected from 15 ELISA detectable subjects that were subjected to either the oral administration of BmrhGM-CSF or the subcutaneous injection of rhGM-CSF. The MS tracings of the 3 subjects as supplementary data were shown in supporting information files ( Table S1, S2, S3 and Figure S1, S2, S3, S4, S5, S6, S7, S8, S9, S10, S11, S12, S13, S14, S15, S16, S17, S18, S19, S20, S21, S22, S23, S24, S25, S26, S27, S28 ). Here, serum MS tracing from one of the 3 volunteers was briefly described as follows:
Using the 0 hour MS data as control, the results of Enhanced Mass Spectrometry (EMS) and EPI analysis suggested that there were differential peaks of the mass-to-electric charge ratio in the serum samples after the oral administration of BmrhGM-CSF or injection of rhGM-CSF (Table 2 and Table 3). Peptide mapping based on the molecular weights demonstrated the presence of hGM-CSF peptide fragments in the differential peaks (Figure 3 and Figure 4). The molecular weights of those different polypeptides were ranged from 2,039 to 7,336Da, which indicated that orally administered BmrhGM-CSF could be absorbed into the blood after penetrated through the intestinal tract.
A) A mass spectrometry profile of one serum subject's sample after oral administration of BmrhGM-CSF at 0 h. B) A mass spectrometry profile of one subject's serum sample after 3 h of the oral administration of BmrhGM-CSF. The arrow indicates the differential point between A and B. C) An amino acid sequence determined by EPI analysis corresponding to the differential point in one subject's serum sample after 3 h of the oral administration of BmrhGM-CSF in comparison to the hGM-CSF sequence. The SP sequence in the pane is the amino acid sequence corresponding to the differential point.
A) A mass spectrometry profile of the serum sample after subcutaneous injection of rhGM-CSF at 0 h. B) A mass spectrometry profile of one subject's serum sample after 3 h of the subcutaneous injection of rhGM-CSF. The arrow indicates the differential point between A and B. C) Amino acid sequence determined by EPI analysis corresponding to the differential point in the subject's serum sample after 3 h of the subcutaneous injection of rhGM-CSF in comparison to the hGM-CSF sequence. The TM sequence in the pane is the amino acid sequence corresponding to the differential point.
An oral administration of protein drugs was considered as a focus area in the study of biological pharmaceuticals worldwide. To date, authentic oral administration of protein drugs has not yet been successfully achieved. Most cytokines and proteins including hGM-CSF, interferon and insulin, were found to be effective when delivered by either intramuscular or subcutaneous injection. If these drugs could be effectively administered through the oral administration in clinical settings, the biological pharmaceuticals industry would be revolutionized.
Several challenges could be encountered in the effective oral administration of protein and cytokine drugs which include a poor intrinsic permeability, a hostile proteolytic environment in the gastrointestinal tract, effects of the liver, and short in vivo half-lives  . Many pharmacologists have been trying to solve these problems. Previous methods for the oral administration of vulnerable pharmacological agents relied on the co-administration of adjuvants (e.g., resorcinol and nonionic surfactants such as polyoxyethylene oleyl ether and n-hexadecyl polyethylene ether) to artificially increase the permeability of the intestina1 walls. Enzymatic inhibitors such as pancreatic trypsin inhibitor and trasylol were also co-administered to inhibit enzymatic degradation . Liposome or microsphere was also used as drug delivery systems for insulin and heparin  . Over the past few decades, significant efforts have been made to develop effective oral peptide and protein formulations, and these have met with various degrees of success. Some modified polypeptides or cytokines such as rIL-12, Ile-Pro-[14C] Pro, rhG-CSF and insulin were shown to be active after oral administration in animal models , –. Several oral preparations of polypeptides and cytokines such as Colostrinin and interferon-alpha have been or still are in a clinical research phase –. However, the bioavailability of protein and cytokine drugs after oral administration in human has rarely been reported.
Foreign genes have been expressed in high level in the silkworm bioreactor. The expressed products possess native-like properties. Additionally, the expressed proteins could be suitably phosphorylated and glycosylated in the bioreactor ,  . Silkworm pupa also harbors an abundance of liposome containing protease inhibitors that protect recombinant proteins from degradation in the gastrointestinal tract –. That allows increased absorption of protein drugs and cytokines, for example, BmrhGM-CSF after the oral administration.
The development of protein drugs that could survive the journey through the gastrointestinal (GI) tract, and then penetrate the bloodstream of the body is a major issue in the pharmaceutical field. Several kinds of protein drugs for oral administration have been genetically engineered. Those include liposome-encapsulated proteins, nanosphere conjugated proteins and fusion proteins which facilitate absorption through the GI tract , –,  . Yet, most of studies are still processing in the stage of animal studies – . It is important to provide experimental proofs at the molecular level to support the theory for the effectiveness of orally administered cytokine drugs or proteins in clinical settings. To achieve this goal, we have carried out a number of preclinical and clinical studies. Here we specifically discuss the clinical data on the bioavailability of BmrhGM-CSF:
In the bioavailability trial, ELISA was used to determine the hGM-CSF concentrations in sera. Using the 19 volunteers, the average hGM-CSF concentration reached its plateau level at 2 h after the oral administration of a single dose of BmrhGM-CSF. The average bioavailability was approximately 1%, and the highest of 3.1%. The blood hGM-CSF concentrations of 19 volunteers were detected by ELISA before and after oral administration of BmrhGM-CSF, but it was not detected in 4 of the 19 ones. This indicated that BmrhGM-CSF could not be absorbed by 4 of 19 subjects. However, BmrhGM-CSF could be absorbed by 79% subjects tested. This might result from individual differences.
The result of MS analysis demonstrated that both small and large hGM-CSF peptide fragments were absorbed into the blood after the oral administration of BmrhGM-CSF, which is in accordance with that of an isotope hybridization test .
In this study, we developed a method for the oral administration of protein or cytokine drugs expressed in the silkworm (B. mori) bioreactor. The absorption of orally administered rhGM-CSF produced in B. mori bioreactor was acceptable, indicating that BmrhGM-CSF may have potential clinical applications. This paper may provide an approach for the oral administration of cytokine and protein drugs.
Bioavailability of orally administered BmrhGM-CSF in healthy volunteers.
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CONSORT Checklist STUDY: Bioavailability of Orally Administered BmrhGM-CSF.
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Subject NO 1:Table. EMS, EPI and Peptide mass fingerprinting detection results of rhGM-CSF in the plasma after either the oral administration of BmrhGM-CSF or the subcutaneous injection of hGM-CSF.
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Subject NO 2:Table. EMS, EPI and Peptide mass fingerprinting detection results of rhGM-CSF in the plasma after either the oral administration of BmrhGM-CSF or the subcutaneous injection of hGM-CSF.
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Subject NO 3:Table. EMS, EPI and Peptide mass fingerprinting detection results of rhGM-CSF in the plasma after either the oral administration of BmrhGM-CSF or the subcutaneous injection of hGM-CSF.
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This clinical trial was approved by the State Food and Drug Administration (SFDA) of China in 2003 (No. 2003L02511), and completed in Second Affiliated Hospital of Zhejiang University. We thank Professor Zeqi Zhou and Professor Yu Zhao for revising the manuscript.
Conceived and designed the experiments: XW YZ. Analyzed the data: ZN JC QS. Wrote the paper: WZ ZL YJ. Supervised laboratory and clinical work: WZ ZL. Enrolled participants: GC WY.
- 1. Gasson JC (1991) Molecular physiology of granulocyte-macrophage colony-stimulating factor. Blood 77: 1131–1145.JC Gasson1991Molecular physiology of granulocyte-macrophage colony-stimulating factor.Blood7711311145
- 2. Vadhan-Raj S, Keating M, LeMaistre A, Hittelman WN, McCredie K, et al. (1987) Effects of recombinant human granulocyte-macrophage colony-stimulating factor in patients with myelodysplastic syndromes. N Engl J Med 317: 1545–1552.S. Vadhan-RajM. KeatingA. LeMaistreWN HittelmanK. McCredie1987Effects of recombinant human granulocyte-macrophage colony-stimulating factor in patients with myelodysplastic syndromes.N Engl J Med31715451552
- 3. Antman KS, Griffin JD, Elias A, Socinski MA, Ryan L, et al. (1988) Effect of recombinant human granulocyte-macrophage colony-stimulating factor on chemotherapy-induced myelosuppression. N Engl J Med 319: 593–598.KS AntmanJD GriffinA. EliasMA SocinskiL. Ryan1988Effect of recombinant human granulocyte-macrophage colony-stimulating factor on chemotherapy-induced myelosuppression.N Engl J Med319593598
- 4. Hord JD, Gay JC, Whitlock JA, Janco RL, Edwards JR, et al. (1995) Long-term granulocyte-macrophage colony-stimulating factor and immunosuppression in the treatment of acquired severe aplastic anemia. J Pediatr Hematol Oncol 17: 140–144.JD HordJC GayJA WhitlockRL JancoJR Edwards1995Long-term granulocyte-macrophage colony-stimulating factor and immunosuppression in the treatment of acquired severe aplastic anemia.J Pediatr Hematol Oncol17140144
- 5. Badaró R, Nascimento C, Carvalho JS, Badaro F, Russo D, et al. (1994) Recombinant human granulocyte-macrophage colony-stimulating factor reverses neutropenia and reduces secondary infections in visceral leishmaniasis. J Infect Dis 170: 413–418.R. BadaróC. NascimentoJS CarvalhoF. BadaroD. Russo1994Recombinant human granulocyte-macrophage colony-stimulating factor reverses neutropenia and reduces secondary infections in visceral leishmaniasis.J Infect Dis170413418
- 6. Hardy D, Spector S, Polsky B, Crumpacker C, Van der Horst C, et al. (1994) Combination of ganciclovir and granulocyte-macrophage colony-stimulating factor in the treatment of cytomegalovirus retinitis in AIDS patients. Eur J Clin Microbiol Infect Dis 13: S34–S40.D. HardyS. SpectorB. PolskyC. CrumpackerC. Van der Horst1994Combination of ganciclovir and granulocyte-macrophage colony-stimulating factor in the treatment of cytomegalovirus retinitis in AIDS patients.Eur J Clin Microbiol Infect Dis13S34S40
- 7. Chen J, Wu XF, Zhang YZ (2006) Expression, purification and characterization of human GM-CSF using silkworm pupae (Bombyx mori) as a bioreactor. J Biotechnol 123: 236–247.J. ChenXF WuYZ Zhang2006Expression, purification and characterization of human GM-CSF using silkworm pupae (Bombyx mori) as a bioreactor.J Biotechnol123236247
- 8. Hussein AM, Ross M, Vredenburgh J, Meisenberg B, Hars V, et al. (1995) Effects of granulocyte-macrophage colony stimulating factor produced in Chinese hamster ovary cells (regramostim), Escherichia coli (molgramostim) and yeast (sargramostim) on priming peripheral blood progenitor cells for use with autologous bone marrow after high-dose chemotherapy. Eur J Haematol 55: 348–356.AM HusseinM. RossJ. VredenburghB. MeisenbergV. Hars1995Effects of granulocyte-macrophage colony stimulating factor produced in Chinese hamster ovary cells (regramostim), Escherichia coli (molgramostim) and yeast (sargramostim) on priming peripheral blood progenitor cells for use with autologous bone marrow after high-dose chemotherapy.Eur J Haematol55348356
- 9. Krumwieh D, Weinmann E, Seiler FR (1988) Human recombinant derived IL-3 and GM-CSF in hematopoiesis of normal cynomolgus monkeys. Behring Inst Mitt 83: 250–257.D. KrumwiehE. WeinmannFR Seiler1988Human recombinant derived IL-3 and GM-CSF in hematopoiesis of normal cynomolgus monkeys.Behring Inst Mitt83250257
- 10. Zhang YZ, Chen J, Lv ZB, Nie ZM, Zhang XY, et al. (2006) Can 29 kDa rhGM-CSF expressed by silkworm pupae bioreactor bring into effect as active cytokine through orally administration? Eur J Pharmaceut Sci 28: 212–223.YZ ZhangJ. ChenZB LvZM NieXY Zhang2006Can 29 kDa rhGM-CSF expressed by silkworm pupae bioreactor bring into effect as active cytokine through orally administration?Eur J Pharmaceut Sci28212223
- 11. Chen J, Nie ZM, Lv ZB, Zhu CG, Xu CZ, et al. (2007) Large-scale purification of human granulocyte-macrophage colony-stimulating factor expressed in Bombyx mori pupae. Appl Biochem Biotechnol 141: 149–160.J. ChenZM NieZB LvCG ZhuCZ Xu2007Large-scale purification of human granulocyte-macrophage colony-stimulating factor expressed in Bombyx mori pupae.Appl Biochem Biotechnol141149160
- 12. (2003) 2003Guidance for Industry. Bioavailability and bioequivalence studies for orally administered drug products general considerations. In: US Department of Health and Human Services. US Food and Drug Administration CfDEaRC, editor. http://www.fdagov/cder/guidance/5356fnlpdf. Guidance for Industry. Bioavailability and bioequivalence studies for orally administered drug products general considerations. In: US Department of Health and Human Services. US Food and Drug Administration CfDEaRC, editor. http://www.fdagov/cder/guidance/5356fnlpdf.
- 13. Schuirmann DJ (1987) A comparison of the two one-sided tests procedure and the power approach for assessing the equivalence of average bioavailability. J Pharmacokinet Biopharm 15: 657–680.DJ Schuirmann1987A comparison of the two one-sided tests procedure and the power approach for assessing the equivalence of average bioavailability.J Pharmacokinet Biopharm15657680
- 14. Chalasani KB, Russell GJ, Yandrapu SK, Diwan PV, Jain SK (2007) A novel vitamin B12-nanosphere conjugate carrier system for peroral delivery of insulin. J Control Rel 117: 421–429.KB ChalasaniGJ RussellSK YandrapuPV DiwanSK Jain2007A novel vitamin B12-nanosphere conjugate carrier system for peroral delivery of insulin.J Control Rel117421429
- 15. T Borchardt R, Aubé Jeffrey, Siahaan TJ, Gangwar S, Pauletti GM (1997) Improvement of oral peptide bioavailability: Peptidomimetics and prodrug strategies. Adv Drug Deliv Rev 27: 235–256.R. T BorchardtJeffrey AubéTJ SiahaanS. GangwarGM Pauletti1997Improvement of oral peptide bioavailability: Peptidomimetics and prodrug strategies.Adv Drug Deliv Rev27235256
- 16. Mathiowitz E, Jacob JS, Jong YS, Carino GP, Chickering DE, et al. (1997) Biologically erodable microspheres as potential oral drug delivery systems. Nature 386: 410–414.E. MathiowitzJS JacobYS JongGP CarinoDE Chickering1997Biologically erodable microspheres as potential oral drug delivery systems.Nature386410414
- 17. Lee SY, Huang CK, Zhang TF, Schofield BH, Burks AW, et al. (2001) Oral administration of IL-12 suppresses anaphylactic reactions in a murine model of peanut hypersensitivity. Clin Immunol 101: 220–228.SY LeeCK HuangTF ZhangBH SchofieldAW Burks2001Oral administration of IL-12 suppresses anaphylactic reactions in a murine model of peanut hypersensitivity.Clin Immunol101220228
- 18. Marinaro M, Boyaka PN, Finkelman FD, Kiyono H, Jackson RJ, et al. (1997) Oral but not parenteral interleukin (IL)-12 redirects T helper 2 (Th2)-type responses to an oral vaccine without altering mucosal IgA responses. J Exp Med 185: 415–427.M. MarinaroPN BoyakaFD FinkelmanH. KiyonoRJ Jackson1997Oral but not parenteral interleukin (IL)-12 redirects T helper 2 (Th2)-type responses to an oral vaccine without altering mucosal IgA responses.J Exp Med185415427
- 19. Jauhiainen T, Wuolle K, Vapaatalo H, Kerojoki O, Nurmela K, et al. (2007) Oral absorption, tissue distribution and excretion of a radiolabelled analog of a milk-derived antihypertensive peptide, Ile-Pro-Pro, in rats. Int Dairy J 17: 1216–1223.T. JauhiainenK. WuolleH. VapaataloO. KerojokiK. Nurmela2007Oral absorption, tissue distribution and excretion of a radiolabelled analog of a milk-derived antihypertensive peptide, Ile-Pro-Pro, in rats.Int Dairy J1712161223
- 20. Gersting JA, Kotto-Kome CA, Dua Y, Christensen RD, Calhoun DA (2003) Bioavailability of granulocyte colony-stimulating factor administered enterally to suckling mice. Pharmacological Res 48: 643–647.JA GerstingCA Kotto-KomeY. DuaRD ChristensenDA Calhoun2003Bioavailability of granulocyte colony-stimulating factor administered enterally to suckling mice.Pharmacological Res48643647
- 21. Leszek J, Inglot AD, Janusz M, Lisowski J, Krukowska K, et al. (1999) Colostrinin: a proline-rich polypeptide (PRP) complex isolated from ovine colostrum for treatment of Alzheimer's disease. A double-blind, placebo-controlled study. Arch Immunol Ther Exp (Warsz) 47: 377–385.J. LeszekAD InglotM. JanuszJ. LisowskiK. Krukowska1999Colostrinin: a proline-rich polypeptide (PRP) complex isolated from ovine colostrum for treatment of Alzheimer's disease. A double-blind, placebo-controlled study.Arch Immunol Ther Exp (Warsz)47377385
- 22. Leszek J, Inglot AD, Janusz M, Byczkiewicz F, Kiejna A, et al. (2002) Colostrinin proline-rich polypeptide complex from ovine colostrum–a long-term study of its efficacy in Alzheimer's disease. Med Sci Monit 8: 193–196.J. LeszekAD InglotM. JanuszF. ByczkiewiczA. Kiejna2002Colostrinin proline-rich polypeptide complex from ovine colostrum–a long-term study of its efficacy in Alzheimer's disease.Med Sci Monit8193196
- 23. Naylor PH, Naylor CW, Hendrix S, Leveque FG (1999) Oral administration of interferon-alpha induces a transient decline in oral mucosal immunoglobulins and an increase in interleukin-5. J Interferon Cytokine Res 19: 953–959.PH NaylorCW NaylorS. HendrixFG Leveque1999Oral administration of interferon-alpha induces a transient decline in oral mucosal immunoglobulins and an increase in interleukin-5.J Interferon Cytokine Res19953959
- 24. Gong ZH, Jin YF, Zhang YZ (2005) Oral administration of a cholera toxin B subunit-insulin fusion protein produced in silkworm protects against autoimmune diabetes. J Biotechnol 119: 93–105.ZH GongYF JinYZ Zhang2005Oral administration of a cholera toxin B subunit-insulin fusion protein produced in silkworm protects against autoimmune diabetes.J Biotechnol11993105
- 25. Miller LK (1988) Baculoviruses as gene expression vectors. Annu Rev Microbiol 42: 177–199.LK Miller1988Baculoviruses as gene expression vectors.Annu Rev Microbiol42177199
- 26. Lu M, Farrell PJ, Johnson R, Iatrou K (1997) A baculovirus (Bombyx mori nuclear polyhedrosis virus) repeat element functions as a powerful constitutive enhancer in transfected insect cells. J Biol Chem 272: 30724–30728.M. LuPJ FarrellR. JohnsonK. Iatrou1997A baculovirus (Bombyx mori nuclear polyhedrosis virus) repeat element functions as a powerful constitutive enhancer in transfected insect cells.J Biol Chem2723072430728
- 27. Shrivastava B, Ghosh AK (2003) Protein purification, cDNA cloning and characterization of a protease inhibitor from the Indian tasar silkworm, Antheraea mylitta. Insect Biochem Mol Biol 33: 1025–1033.B. ShrivastavaAK Ghosh2003Protein purification, cDNA cloning and characterization of a protease inhibitor from the Indian tasar silkworm, Antheraea mylitta.Insect Biochem Mol Biol3310251033
- 28. He N, Yakiyama M, Fujii H, Banno Y, Yamamoto K (2003) Genomic structure and expression analysis of the gene encoding a silkworm basic Kunitz-type chymotrypsin inhibitor. Biochim Biophys Acta 1628: 71–77.N. HeM. YakiyamaH. FujiiY. BannoK. Yamamoto2003Genomic structure and expression analysis of the gene encoding a silkworm basic Kunitz-type chymotrypsin inhibitor.Biochim Biophys Acta16287177
- 29. Shiba H, Uchida D, Kobayashi H, Natori M (2001) Involvement of cathepsin B- and L-like proteinases in silk gland histolysis during metamorphosis of Bombyx mori. Arch Biochem Biophys 390: 28–34.H. ShibaD. UchidaH. KobayashiM. Natori2001Involvement of cathepsin B- and L-like proteinases in silk gland histolysis during metamorphosis of Bombyx mori.Arch Biochem Biophys3902834
- 30. Shirai K, Fujii H, Doira H, Iwamoto H (2000) Synthesis and resorption of a humoral chymotrypsin inhibitor, CI-8, by fat body of the silkworm, Bombyx mori. Insect Biochem Mol Biol 30: 363–368.K. ShiraiH. FujiiH. DoiraH. Iwamoto2000Synthesis and resorption of a humoral chymotrypsin inhibitor, CI-8, by fat body of the silkworm, Bombyx mori.Insect Biochem Mol Biol30363368
- 31. Yamamoto Y, Watabe S, Kageyama T, Takahashi SY (1999) A novel inhibitor protein for Bombyx cysteine proteinase is homologous to propeptide regions of cysteine proteinases. FEBS Lett 448: 257–260.Y. YamamotoS. WatabeT. KageyamaSY Takahashi1999A novel inhibitor protein for Bombyx cysteine proteinase is homologous to propeptide regions of cysteine proteinases.FEBS Lett448257260
- 32. Sasaki T (1978) Chymotrypsin inhibitors from hemolymph of the silkworm, Bombyx mori. J Biochem 84: 267–276.T. Sasaki1978Chymotrypsin inhibitors from hemolymph of the silkworm, Bombyx mori.J Biochem84267276