This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Jertborn, M.
Right arrow Articles by Svennerholm, A.-M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jertborn, M.
Right arrow Articles by Svennerholm, A.-M.

 Previous Article  |  Next Article 

Clinical and Diagnostic Laboratory Immunology, March 2001, p. 424-428, Vol. 8, No. 2
1071-412X/01/$04.00+0   DOI: 10.1128/CDLI.8.2.424-428.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Dose-Dependent Circulating Immunoglobulin A Antibody-Secreting Cell and Serum Antibody Responses in Swedish Volunteers to an Oral Inactivated Enterotoxigenic Escherichia coli Vaccine

Marianne Jertborn,1,2,* Christina Åhrén,1,2 and Ann-Mari Svennerholm1

Department of Medical Microbiology and Immunology1 and Department of Infectious Diseases,2 Göteborg University, Göteborg, Sweden

Received 7 June 2000/Returned for modification 15 September 2000/Accepted 9 January 2001


    ABSTRACT
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

The immunogenicity of different preparations of an oral inactivated enterotoxigenic Escherichia coli (ETEC) vaccine was evaluated in Swedish volunteers previously unexposed to ETEC infection. The vaccine preparations consisted of recombinant cholera toxin B subunit (CTB) and various amounts of formalin-killed whole bacteria expressing the most prevalent colonization factor antigens (CFAs). Significant immunoglobulin A (IgA) antibody-secreting cell (ASC) responses against CTB and the various CFA components were seen in a majority of volunteers after two doses of ETEC vaccine independent of the vaccine lot given. The IgA ASC responses against CTB were significantly higher after the second than after the first immunization, whereas the CFA-specific IgA ASC responses were almost comparable after the first and second doses of ETEC vaccine. Two immunizations with one-third of a full dose of CFA-ETEC bacteria induced lower frequencies of IgA ASC responses against all the different CFAs than two full vaccine doses, i.e., 63 versus 80% for CFA/I, 56 versus 70% for CS1, 31 versus 65% for CS2, and 56 versus 75% for CS4. The proportion of vaccinees responding with rises in the titer of serum IgA antibody against the various CFA antigens was also lower after immunization with the reduced dose of CFA-ETEC bacteria. These findings suggest that measurements of circulating IgA ASCs can be used not only for qualitative but also for quantitative assessments of the immunogenicity of individual fimbrial antigens in various preparations of ETEC vaccine.


    INTRODUCTION
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

Enterotoxigenic Escherichia coli (ETEC) is the most common cause of diarrhea among children in developing countries and among international travelers to less-developed areas (4). Because of the high morbidity and mortality attributable to ETEC infections, development of vaccines against ETEC is given a high priority. An effective ETEC vaccine should be given orally and ideally should contain an appropriate toxoid in combination with ETEC bacteria expressing the most important colonization factor antigens (CFAs) in order to stimulate relevant immune responses locally in the intestine (3, 7, 21, 22). Oral immunization with the cholera toxin B subunit (CTB) has been shown to provide significant protection against diarrhea caused by heat-labile enterotoxin-producing E. coli in children in areas where ETEC is endemic as well as in adult travelers (5, 15).

We have developed an oral, inactivated ETEC vaccine consisting of recombinantly produced CTB (rCTB) in combination with five different E. coli strains expressing CFA/I and the different coli surface (CS)-associated subcomponents of CFA/II (CS1 to -3) and CFA/IV (CS4 and -5) in high concentrations and in an immunogenic form on their surfaces (10, 22). Several phase I and phase II trials in different countries have shown that the vaccine is safe and stimulates mucosal immune responses in a majority of vaccinees (1, 10, 16, 18, 19, 23). In most of these studies, the intestine-derived mucosal immunoglobulin A (IgA) immune responses against ETEC vaccine have been assessed by measuring IgA antibody-secreting cells (ASCs) in peripheral blood (10, 16, 18, 19, 23). Monitoring of different homing receptors on circulating ASCs induced by different routes of immunization has shown that ASCs of the IgA isotype assayed 7 days after administration of oral antigen largely represent cells of gut origin (12, 17). Moreover, significant correlations between IgA antibody responses in intestinal lavage fluids and increases in circulating IgA ASCs against CTB and the different CFAs of the ETEC vaccine have recently been demonstrated (2).

The aim of the present study was to compare the immune responses after immunization with one and two doses and with different doses of an oral ETEC vaccine in persons living in an area where ETEC is not endemic. This was done by assessing intestinally derived ASC responses in the peripheral blood and antibody responses in the serum of differently immunized adult Swedish volunteers.


    MATERIALS AND METHODS
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

ETEC vaccines and placebo composition. The different preparations, lots 003 and 005, of an oral ETEC vaccine were produced by SBL Vaccin, Stockholm, Sweden, as previously described (1). One 4-ml dose of vaccine contained 1.0 mg of rCTB and ~1011 formalin-inactivated E. coli bacteria of each of the following strains: SBL101 (O78:H12; CFA/I ST+), SBL104 (O25:H42; CS4), SBL105 (O167:H5; CS5 ST+), SBL 106 (O6:H16; CS1), and SBL 107 (OR:H6; CS2+ CS3) (10, 18, 19). The two vaccine lots contained various amounts of the ETEC fimbrial antigens CFA/I and CS2. Lot 005 contained half the amount of CFA/I and three times more CS2 than lot 003. The 4-ml placebo dose consisted of ~1011 heat-killed E. coli K-12 bacteria.

Each dose of a study agent was administered in 150 ml of a sodium bicarbonate solution (Samarin; Cederroths Nordic AB, Upplands Väsby, Sweden). The volunteers were instructed not to eat or drink (except water) for 1 h before and after intake of the vaccine or placebo preparation.

Study design. Sixty-seven adult Swedish volunteers (32 women), ages 18 to 46, gave informed consent to participate in the studies, which were approved by the Human Research Ethical Committee at the Medical Faculty, Göteborg University. None of the participants had been traveling to areas where ETEC is endemic for 6 months prior to the study.

In the first study, 20 volunteers received two oral immunizations 2 weeks apart with a full dose of ETEC vaccine lot 003, and another 16 volunteers were given two doses of the same vaccine containing one-third of a full dose of CFA-ETEC bacteria and 1 mg of rCTB. Heparinized venous blood (30 ml) for ASC analyses and serum specimens were collected on the day of the first immunization (day 0) and then 7 days after the second vaccine dose. From volunteers receiving the full dose of ETEC vaccine, venous blood samples were also obtained 7 days after the first immunization.

In a second study (performed one year after the first study), the immunogenicity of two doses of a different preparation of ETEC vaccine, lot 005, given 2 weeks apart was investigated in a double-blind, placebo-controlled fashion. Thirty-one subjects were randomly allocated to one of two groups in a 3:2 (vaccine-to-placebo) ratio. Venous blood samples for ASC analyses were collected 7 days after the first and second immunizations, whereas serum specimens were collected on the day of the first immunization (day 0) and then 7 days after each vaccination.

Detection of circulating ASCs. Mononuclear cells (MNCs) from heparinized venous blood were isolated by standard gradient centrifugation on Ficoll-Paque (Pharmacia Biotech AB, Uppsala, Sweden). The numbers of IgA-secreting cells and antigen-specific IgA ASCs were measured by a micromodification of the original enzyme-linked immunospot assay (6, 23). Briefly, individual wells of nitrocellulose-bottomed plates were coated with purified CFA/I (20 µg ml-1), CS1 (10 µg ml-1), CS2 (10 µg ml-1), CS4 (10 µg ml-1), or GM1 ganglioside (5 µg ml-1). The GM1-coated wells were further incubated with purified recombinant CTB (2.5 µg ml-1). After blocking with Iscove's complete medium, the wells were incubated with 5 × 104 to 1 × 106 peripheral blood cells. Specific ASCs were demonstrated by the addition of affinity-purified goat anti-human IgA antibodies conjugated with horseradish peroxidase (Southern Biotechnology Associates, Birmingham, Ala.) followed by enzyme-chromogen substrate. Spots were enumerated under low magnification (×40), and the number of ASCs was calculated as the mean for four wells. Vaccine-specific IgA ASCs were expressed per 107 MNCs to allow comparison with results in other studies (9, 10, 16, 18).

Vaccinees who developed a twofold or greater increase in vaccine-specific IgA ASCs between pre- and postvaccination specimens were regarded as responders on the condition that the number of ASCs exceeded 10 per 107 MNCs in the postvaccination specimens (10). Since preimmune samples were not collected in the second study, these volunteers were considered responders if their postvaccination levels of specific IgA ASCs equaled or exceeded by 2 standard deviations the geometric mean of specific IgA ASCs of placebo recipients examined on the same occassion. Thus, postvaccination values of >10 IgA ASCs per 107 MNCs for CFA/I, >15 IgA ASCs per 107 MNCs for CS1, CS2, and CS4, and >30 IgA ASCs per 107 MNCs for CTB were considered responses.

Serum antibody determinations. Antibodies of the IgA isotype to CTB were measured by the GM1-enzyme-linked immunosorbent assay (ELISA) technique as previously described (1, 8, 20). Antibody responses of the IgA class to CFAs of the vaccine strains in serum were studied by enzyme-linked immunosorbent assay methods (10). In short, individual microtiter wells were coated with 1 µg of purified CFA/I, CS1, CS2, or CS4/ml, respectively. After blocking was done with 0.1% bovine serum albumin, the wells were incubated with threefold serial dilutions of serum samples at room temperature for 90 min. Bound antibodies were demonstrated by addition of human IgA conjugated with horseradish peroxidase (Jackson ImmunoResearch Laboratories, Westgrove, Pa.) and incubated at room temperature for 90 min followed by addition of orthophenylene-diamine (OPD)-H2O2. Titers of antibody were assigned as the interpolated dilutions of the samples giving an absorbance value at 450 nm of 0.4 above background when the wells were allowed to react for 20 min with OPD-H2O2. Pre- and postimmunization specimens from the same subject were always tested side by side. The titer of antibody ascribed to each sample represents the mean of duplicate determinations. A twofold or greater increase in the endpoint titer between pre- and postimmunization specimens was used to signify seroconversion (1, 8).

Statistical analysis. The frequency and magnitude of ASC responses and antibody seroconversion to various immunization schedules and doses of CFA antigens were compared for statistical significance using Fisher's exact test and Student's t test, respectively. All statistical tests were interpreted in a two-tailed fashion.


    RESULTS
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

Comparison of responses after one and two doses. Immune responses to different vaccine antigens after one and two oral immunizations with ETEC vaccine, lot 003, were determined for 20 volunteers. Prior to immunization, the numbers of CFA- and CTB-specific IgA ASCs were low or negligible, i.e., a mean 1 to 4 ASCs per 107 MNCs for each of the various antigens. Significant IgA ASC responses to CFA/I, CS1, CS2, CS4, and CTB were found in 85 to 95% of the vaccinees after either the first or the second dose (Table 1). The frequencies and the magnitudes of the different CFA ASC responses were comparable after the first and the second immunizations, except for the magnitude of the CFA/I response, which was slightly higher after the first dose. There was also a trend of higher median numbers of CFA/I-specific IgA ASCs after the first than after the second vaccine dose, whereas no such difference in the postvaccination levels of IgA ASCs against CS1, CS2, and CS4 was noted (Table 1). The magnitude of the CTB-specific IgA ASC response was significantly (P < 0.001) higher after the second than after the first vaccination (Table 1).

                              
View this table:
[in this window]
[in a new window]
  		TABLE 1.   Comparison of vaccine-specific IgA ASC responses to CFAs and CTB in the peripheral blood of 20 Swedish volunteers after one and two oral immunizations with the ETEC vaccine (lot 003)

The proportion of volunteers responding to the first dose of vaccine with rises in the titer of specific IgA antibody in serum was further increased by a second dose, i.e., the seroconversion rate was 50% after the first dose versus 65% after the second dose for CFA/I, 0 versus 20% for CS1, 15 versus 40% for CS2, 20 versus 40% for CS4, and 35 versus 95% for CTB. The magnitudes of the different CFA antibody titer increases among responders were similar after the first and second immunizations; i.e., the titer increases were, respectively, 2.3-fold and 3.9-fold for CFA/I, not calculable and 3.2-fold for CS1, 4.5-fold and 4.2-fold for CS2, and 3.0-fold and 3.0-fold for CS4. The increase in the titer of IgA antitoxin, on the other hand, was significantly (P < 0.001) higher after the second (50.1-fold) than after the first (1.6-fold) vaccine dose.

Comparison of responses to various amounts of ETEC bacteria. Vaccine-specific IgA ASCs and IgA antibody responses in serum were also monitored in 16 volunteers after two oral doses with ETEC vaccine lot 003 containing one-third of a full dose of CFA-ETEC bacteria and 1 mg of rCTB. The immune responses were compared with those found in the above-mentioned group of 20 volunteers given two immunizations with a full dose of ETEC vaccine lot 003. The number of vaccinees responding with circulating IgA ASCs against the different CFAs, i.e., CFA/I, CS1, CS2, and CS4, was lower after immunization with one-third versus a full dose of ETEC bacteria (Fig. 1). The increase in the numbers of IgA ASCs per 107 MNCs was, as a mean, 14.5-fold after the reduced dose versus 28.8-fold after the full dose of ETEC bacteria for CFA/I, 5.8-fold versus 8.7-fold for CS1, 5.9-fold versus 10.5-fold for CS2, and 4.6-fold versus 10.0-fold for CS4. Also, the median postvaccination levels of IgA ASCs were considerably lower in the group of volunteers given the reduced dose of CFA-ETEC bacteria for all tested CFA antigens except CFA/I (Fig. 1); the differences were statistically significant (P < 0.05) for CS1 and CS2.


View larger version (30K):
[in this window]
[in a new window]
  		FIG. 1.   Vaccine-specific IgA ASC responses to various CFAs in the peripheral blood of Swedish volunteers 7 days after two oral immunizations with a full dose () and a one-third dose (), respectively, of the whole-cell component of ETEC vaccine (lot 003); both preparations contained 1 mg of rCTB. The median numbers of vaccine-specific IgA ASCs per 107 MNCs are shown; values are based on quadruplicate determinations. Percentages of volunteers with significantly (i.e., >=  twofold) higher numbers of IgA ASCs after the second vaccine dose than before immunization are indicated above the bars.

The proportion of vaccinees responding with rises in the titer of IgA antibody against CFA/I, CS1, CS2, and CS4 in serum was also lower for volunteers receiving the reduced versus the full dose of CFA-ETEC bacteria, whereas the magnitudes of the increases in the titer of antibody were comparable for the two immunization groups (Table 2).

                              
View this table:
[in this window]
[in a new window]
  		TABLE 2.   IgA antibody responses in serum before and after two oral immunizations with different doses of the whole-cell component of the ETEC vaccine (lot 003)

Comparison of CFA responses in vaccine and placebo recipients. The immunogenicity of a different preparation of ETEC vaccine, lot 005, was assessed in a placebo-controlled study by measuring circulating IgA ASCs and the IgA antibody responses in serum for 31 volunteers after one and two doses. Based on results from the dose-finding study of ETEC vaccine lot 003, the content of CFA/I was decreased and that of CS2 was increased in lot 005. Most of the vaccinees (63 to 95%) exhibited significant IgA ASC responses to CFA/I, CS1, CS2, and CS4 7 days after either the first or the second immunization with ETEC vaccine, compared with 8% or less for the placebo recipients (P < 0.05 for each vaccine-placebo comparison) (Table 3). In analogy with our previous finding, the responses of circulating IgA ASCs to the different CFA antigens were comparable or slightly stronger after the first than after the second immunization (data not shown). The frequencies and the median postvaccination levels of the CFA- and CTB-specific IgA ASC responses did not differ significantly for the two vaccine lots, even though lot 005 contained half as much CFA/I and approximately three times more CS2 than lot 003. 

                              
View this table:
[in this window]
[in a new window]
  		TABLE 3.   CFA-specific responses of IgA ASCs in blood and IgA antibodies in serum of healthy Swedish volunteers after either one or two oral doses of the ETEC vaccine (lot 005) or E. coli K-12 placebo

In serum, a twofold or greater increase in the titer of IgA antibody against CFA/I, CS1, CS2, and CS4 was found in, respectively, 84, 21, 53, and 63% of the vaccinees after either the first or second vaccine dose, compared with 8% or less for the placebo recipients (Table 3). The seroconversion rate was always higher after the second than after the first immunization for each of the various CFA antigens, whereas the magnitudes of the increases in the titer of antibody among responders were comparable (data not shown). Both the frequencies and the magnitudes of the serological responses were similar after immunization with ETEC vaccine lots 003 and 005.


    DISCUSSION
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

In this study we show for the first time that CFA responses after oral immunization with ETEC vaccine are clearly dose dependent. We also show that the CFA-specific IgA ASC responses in peripheral blood are almost comparable after the first and second immunizations in nonprimed individuals. These findings contrast with the much higher CFA ASC responses found after one than after two doses of ETEC vaccine for persons who have been primed by previous exposure to ETEC antigens (16, 18).

The present study of various preparations of an oral ETEC vaccine confirms and extends the findings from our previous trials of the oral inactivated ETEC vaccine in adult Swedish volunteers (1, 10, 23). Significant IgA ASC responses against CTB and the various CFA components of the vaccine were seen in a majority of volunteers after immunization with two different lots, 003 and 005, of an oral ETEC vaccine containing various amounts of the same CFA-expressing bacterial strains together with recombinant CTB. The mucosal immune responses did not differ significantly for the two vaccine preparations, even though lot 005 contained half the amount of CFA/I and three times more CS2-expressing bacteria than lot 003. However, our small dose-finding study of the ETEC vaccine showed a clear trend toward lower frequencies and magnitudes of circulating IgA ASC responses against all the different CFAs after administration of a vaccine preparation containing one-third of the original dose of CFA-ETEC bacteria. Also, the proportion of volunteers responding with rises in the titer of IgA antibody in serum against CFA/I, CS1, CS2, and CS4 was lower after immunization with one-third than with a full dose of ETEC bacteria. The impaired immunogenicity was most pronounced for CS1 and CS2, i.e., the fimbrial antigens of lowest content in the vaccine preparation. Our findings indicate that there is a relation between the mucosal responsiveness and the content of individual CFA and CS components of the ETEC vaccine, but only up to a certain level, above which administration of more fimbrial antigen did not result in any further increase in the immune response. Thus, measurements of circulating IgA ASCs seem to be of value not only for qualitative but also for quantitative assessments of the immunogenicity of individual fimbrial antigens in various preparations of the ETEC vaccine.

An important aspect of our study was to determine when the peak immune responses after ETEC vaccination appear in volunteers who have not been previously exposed to ETEC infection. According to several studies, IgA ASC responses in blood peak after primary immunization with oral live vaccines against cholera, typhoid fever, and Shigella flexneri infection (12, 13, 14). This was also the case when the oral inactivated ETEC vaccine was given to Egyptian and Bangladeshi adults endemically exposed to ETEC infection (16, 18). In all cases the CFA-specific IgA ASC responses were greater (18) or considerably greater (16) after the first than after the second vaccine dose. In contrast to these reports, we found that the frequencies and the magnitudes of circulating IgA ASC responses against the various CFA antigens in adult Swedish volunteers were comparable (or almost comparable for CFA/I) after the first and second immunizations with ETEC vaccine (both lots). In contrast, the CTB-specific IgA ASC responses and the increases in the titer of IgA antitoxin in serum were significantly higher after the second than after the first vaccination. This pattern in antitoxin responses was consistent with those in previous trials of the oral ETEC vaccine and with results from studies with the oral inactivated B subunit-whole cell cholera vaccine in nonprimed individuals (9, 23).

When evaluating the immunogenicity of enteric vaccines, it is important to determine whether responses to the vaccines of persons living in an area where the disease is not endemic will be similar to responses of residents in areas where it is endemic. Hitherto, three randomized, double-blinded, placebo-controlled trials of the oral ETEC vaccine have been performed with Egyptian adults (18) and children ages 2 to 12 years (19) living in areas where ETEC infections are highly endemic. The present study was designed to assess the immunogenicity of the oral ETEC vaccine, containing the same CFA-expressing bacteria as the vaccine lot used in the Egyptian studies, in persons who had not been primed by previous natural exposure to ETEC antigens. The cumulative proportion of volunteers responding with circulating IgA ASCs to either a first or a second dose of ETEC vaccine was found to be somewhat lower in the Swedish than in the Egyptian studies for all vaccine-related CFA antigens except CS1. The observed differences in the various studies might be explained by the fact that most Egyptian subjects probably had already experienced infection with ETEC before vaccination, and their immune responses to ETEC vaccine may, in part, have represented anamnestic responses. Whether immunologically naive infants in developing countries (the main target group for ETEC vaccination) will respond to the oral ETEC vaccine in a manner similar to that of Swedish adults previously unexposed to ETEC infection still remains to be investigated.


    ACKNOWLEDGMENTS

We are grateful to Marie Andersson, Camilla Johansson, and Gudrun Wiklund for skillful technical assistance and to SBL Vaccin AB, Stockholm, Sweden, for providing the different preparations of ETEC vaccine.

This study was supported by grants from the Swedish Research Council (grant 16X-09084), the Swedish Agency for Research Cooperation with Developing Countries, the World Health Organization, and the Medical Faculty, Göteborg University.


    FOOTNOTES

* Corresponding author. Mailing address: Department of Medical Microbiology and Immunology, Göteborg University, Guldhedsgatan 10, 413 46 Göteborg, Sweden. Phone: 46-31-3424614. Fax: 46-31-826976. E-mail: marianne.jertborn{at}microbio.gu.se.


    REFERENCES
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

1. Åhrén, C., C. Wennerås, J. Holmgren, and A.-M. Svennerholm. 1993. Intestinal antibody response after oral immunization with a prototype cholera B subunit-colonization factor antigen enterotoxigenic Escherichia coli vaccine. Vaccine 11:929-934[CrossRef][Medline].
2. Åhrén, C., M. Jertborn, and A.-M. Svennerholm. 1998. Intestinal immune responses to an inactivated oral enterotoxigenic Escherichia coli vaccine and associated immunoglobulin A responses in blood. Infect. Immun. 66:3311-3316[Abstract/Free Full Text].
3. Åhrén, C. M., and A.-M. Svennerholm. 1982. Synergistic protective effect of antibodies against enterotoxigenic Escherichia coli enterotoxin and colonization factor antigens. Infect. Immun. 38:74-79[Abstract/Free Full Text].
4. Black, R. E. 1993. The epidemiology of diarrheal disease: implications for control by vaccines. Vaccine 11:100-106[CrossRef][Medline].
5. Clemens, J. D., D. A. Sack, J. R. Harris, J. Chakraborty, P. K. Neogy, B. Stanton, N. Huda, M. U. Khan, B. A. Kay, M. R. Khan, M. Ansaruzzaman, M. Yunus, M. R. Rao, A.-M. Svennerholm, and J. Holmgren. 1988. Cross-protection by B subunit-whole cell cholera vaccine against diarrhea associated with heat-labile toxin-producing enterotoxigenic Escherichia coli: results of a large-scale field trial. J. Infect. Dis. 158:372-377[Medline].
6. Czerkinsky, C., L.-Å. Nilsson, H. Nygren, Ö. Ouchterlony, and A. A. Tarkowski. 1983. Solid-phase enzyme-linked immunospot (ELISPOT) assay for enumeration of specific antibody-secreting cells. J. Immunol. Methods 65:109-121[CrossRef][Medline].
7. Czerkinsky, C., A.-M. Svennerholm, and J. Holmgren. 1993. Induction and assessment of immunity at enteromucosal surfaces in humans: implications for vaccine development. Clin. Infect. Dis. 16(Suppl. 2):106-116.
8. Jertborn, M., A.-M. Svennerholm, and J. Holmgren. 1986. Saliva, breast milk and serum antibody responses as indirect measures of intestinal immunity after oral cholera vaccination or natural disease. J. Clin. Microbiol. 24:203-209[Abstract/Free Full Text].
9. Jertborn, M., A.-M. Svennerholm, and J. Holmgren. 1994. Immunological memory after immunization with oral cholera B subunit-whole-cell vaccine in Swedish volunteers. Vaccine 12:1078-1082[CrossRef][Medline].
10. Jertborn, M., C. Åhrén, J. Holmgren, and A.-M. Svennerholm. 1998. Safety and immunogenicity of an oral inactivated enterotoxigenic Escherichia coli vaccine. Vaccine 16:255-260[CrossRef][Medline].
11. Kantele, A., J. M. Kantele, H. Arvilommi, and P. H. Mäkele. 1991. Active immunity is seen as a reduction in the cell response to oral live vaccine. Vaccine 9:428-431[CrossRef][Medline].
12. Kantele, A., M. Häkkinen, Z. Moldoveanu, A. Lu, E. Savilahti, R. D. Alvarez, S. Michalek, and J. Mestecky. 1998. Differences in immune responses induced by oral and rectal immunizations with Salmonella typhi Ty21a: evidence for compartmentalization within the common mucosal immune system in humans. Infect. Immun. 66:5630-5635[Abstract/Free Full Text].
13. Li, A., T. Pal, U. Forsum, and A. A. Lindberg. 1992. Safety and immunogenicity of the live oral auxotrophic Shigella flexneri SFL 124 in volunteers. Vaccine 10:395-404[CrossRef][Medline].
14. Losonsky, G. A., C. O. Tacket, S. S. Wasserman, J. B. Kaper, and M. Levine. 1993. Secondary Vibrio cholerae-specific cellular antibody responses following wild-type homologous challenge in people vaccinated with CVD 103-HgR live oral cholera vaccine: changes with time and lack of correlation with protection. Infect. Immun. 61:729-733[Abstract/Free Full Text].
15. Peltola, H., A. Siitonen, H. Kyrönseppä, I. Simula, L. Mattila, P. Oksanen, M. J. Kataja, and M. Cadoz. 1991. Prevention of travellers' diarrhoea by oral B-subunit/whole-cell cholera vaccine. Lancet 338:1285-1289[CrossRef][Medline].
16. Qadri, F., C. Wennerås, F. Ahmed, M. Asaduzzaman, D. Saha, M. J. Albert, R. B. Sack, and A.-M. Svennerholm. 2000. Safety and immunogenicity of an oral, inactivated enterotoxigenic Escherichia coli plus cholera toxin B subunit vaccine in Bangladeshi adults and children. Vaccine 18:2704-2712[CrossRef][Medline].
17. Quiding-Järbrink, M., I. Nordström, G. Granström, A. Kilander, M. Jertborn, E. C. Butcher, A. I. Lazarovits, J. Holmgren, and C. Czerkinsky. 1997. Differential expression of tissue-specific adhesion molecules on human circulating antibody-forming cells after systemic, enteric and nasal immunisations. A molecular basis for the compartmentalization of effector B cell responses. J. Clin. Investig. 99:1281-1286[Medline].
18. Savarino, S. J., F. M. Brown, E. Hall, S. Bassily, F. Youssef, T. Wierzba, L. Peruski, N. A. El-Masry, M. Safwat, M. Rao, M. Jertborn, A.-M. Svennerholm, and J. D. Clemens. 1998. Safety and immunogenicity of an oral, killed enterotoxigenic Escherichia coli-cholera toxin B subunit vaccine in Egyptian adults. J. Infect. Dis. 177:796-799[Medline].
19. Savarino, S. J., E. R. Hall, S. Bassily, F. M. Brown, F. Youssef, T. F. Wierzba, L. Peruski, N. A. El-Masry, M. Safwat, M. Rao, H. El Mohamady, R. Abu-Elyazeed, A. Naficy, A.-M. Svennerholm, M. Jertborn, Y. J. Lee, and J. D. Clemens. 1999. Oral, inactivated, whole cell enterotoxigenic Escherichia coli plus cholera toxin B subunit vaccine: results of the initial evaluation in children. J. Infect. Dis. 179:107-114[CrossRef][Medline].
20. Svennerholm, A.-M., J. Holmgren, R. Black, M. Levine, and M. M. Merson. 1983. Serologic differentiation between antitoxin responses to infection with Vibrio cholerae and enterotoxin-producing Escherichia coli. J. Infect. Dis. 147:514-522[Medline].
21. Svennerholm, A.-M., J. Holmgren, and D. A. Sack. 1989. Development of oral vaccines against enterotoxigenic Escherichia coli diarrhoea. Vaccine 7:196-198[CrossRef][Medline].
22. Svennerholm, A.-M., C. Åhrén, and M. Jertborn. 1997. Vaccines against enterotoxigenic Escherichia coli infections. I. Oral inactivated vaccines against enterotoxigenic Escherichia coli, p. 865-873. In M. M. Levine, G. C. Woodrow, J. B. Kaper, and G. S. Gobon (ed.), New generation vaccines. Marcel Dekker, New York, N.Y.
23. Wennerås, C., A.-M. Svennerholm, C. Åhrén, and C. Czerkinsky. 1992. Antibody-secreting cells in human peripheral blood after oral immunization with an inactivated enterotoxigenic Escherichia coli vaccine. Infect. Immun. 60:2605-2611[Abstract/Free Full Text].

Clinical and Diagnostic Laboratory Immunology, March 2001, p. 424-428, Vol. 8, No. 2
1071-412X/01/$04.00+0   DOI: 10.1128/CDLI.8.2.424-428.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.


This article has been cited by other articles:

  • McKenzie, R., Bourgeois, A. L., Engstrom, F., Hall, E., Chang, H. S., Gomes, J. G., Kyle, J. L., Cassels, F., Turner, A. K., Randall, R., Darsley, M., Lee, C., Bedford, P., Shimko, J., Sack, D. A. (2006). Comparative Safety and Immunogenicity of Two Attenuated Enterotoxigenic Escherichia coli Vaccine Strains in Healthy Adults. Infect. Immun. 74: 994-1000 [Abstract] [Full Text]  
  • Turner, A. K., Beavis, J. C., Stephens, J. C., Greenwood, J., Gewert, C., Thomas, N., Deary, A., Casula, G., Daley, A., Kelly, P., Randall, R., Darsley, M. J. (2006). Construction and Phase I Clinical Evaluation of the Safety and Immunogenicity of a Candidate Enterotoxigenic Escherichia coli Vaccine Strain Expressing Colonization Factor Antigen CFA/I. Infect. Immun. 74: 1062-1071 [Abstract] [Full Text]  
  • Wang, L., Kedzierski, L., Wesselingh, S. L., Coppel, R. L. (2003). Oral Immunization with a Recombinant Malaria Protein Induces Conformational Antibodies and Protects Mice against Lethal Malaria. Infect. Immun. 71: 2356-2364 [Abstract] [Full Text]  
  • Dougan, G., Huett, A., Clare, S. (2002). Vaccines against human enteric bacterial pathogens. Br Med Bull 62: 113-123 [Abstract] [Full Text]  
  • Guerena-Burgueno, F., Hall, E. R., Taylor, D. N., Cassels, F. J., Scott, D. A., Wolf, M. K., Roberts, Z. J., Nesterova, G. V., Alving, C. R., Glenn, G. M. (2002). Safety and Immunogenicity of a Prototype Enterotoxigenic Escherichia coli Vaccine Administered Transcutaneously. Infect. Immun. 70: 1874-1880 [Abstract] [Full Text]  

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Jertborn, M.
Right arrow Articles by Svennerholm, A.-M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jertborn, M.
Right arrow Articles by Svennerholm, A.-M.

Copyright © 2009 by the American Society for Microbiology.   For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»