Comparison of Plasmodium berghei challenge models for the evaluation of pre-erythrocytic malaria vaccines and their effect on perceived vaccine efficacy
© Leitner et al; licensee BioMed Central Ltd. 2010
Received: 16 March 2010
Accepted: 27 May 2010
Published: 27 May 2010
The immunological mechanisms responsible for protection against malaria infection vary among Plasmodium species, host species and the developmental stage of parasite, and are poorly understood. A challenge with live parasites is the most relevant approach to testing the efficacy of experimental malaria vaccines. Nevertheless, in the mouse models of Plasmodium berghei and Plasmodium yoelii, parasites are usually delivered by intravenous injection. This route is highly artificial and particularly in the P. berghei model produces inconsistent challenge results. The initial objective of this study was to compare an optimized intravenous (IV) delivery challenge model with an optimized single infectious mosquito bite challenge model. Finding shortcomings of both approaches, an alternative approach was explored, i.e., the subcutaneous challenge.
Mice were infected with P. berghei sporozoites by intravenous (tail vein) injection, single mosquito bite, or subcutaneous injection of isolated parasites into the subcutaneous pouch at the base of the hind leg. Infection was determined in blood smears 7 and 14 days later. To determine the usefulness of challenge models for vaccine testing, mice were immunized with circumsporozoite-based DNA vaccines by gene gun.
Despite modifications that allowed infection with a much smaller than reported number of parasites, the IV challenge remained insufficiently reliable and reproducible. Variations in the virulence of the inoculum, if not properly monitored by the rigorous inclusion of sporozoite titration curves in each experiment, can lead to unacceptable variations in reported vaccine efficacies. In contrast, mice with different genetic backgrounds were consistently infected by a single mosquito bite, without overwhelming vaccine-induced protective immune responses. Because of the logistical challenges associated with the mosquito bite model, the subcutaneous challenge route was optimized. This approach, too, yields reliable challenge results, albeit requiring a relatively large inoculum.
Although a single bite by P. berghei infected Anopheles mosquitoes was superior to the IV challenge route, it is laborious. However, any conclusive evaluation of a pre-erythrocytic malaria vaccine candidate should require challenge through the natural anatomic target site of the parasite, the skin. The subcutaneous injection of isolated parasites represents an attractive compromise. Similar to the mosquito bite model, it allows vaccine-induced antibodies to exert their effect and is, therefore not as prone to the artifacts of the IV challenge.
Despite decades of research, malaria infection remains a major global health problem with high mortality and morbidity. Efforts to disrupt the life cycle of the parasite by controlling the vector have had only limited success, while the usefulness of anti-malarial drugs is hampered by their lack of availability to those most in need and to the rapid evolution of drug resistant parasites. An effective vaccine remains the most promising approach to controlling the disease , but is still not available.
Research on malaria vaccines is complicated by the lack of surrogate markers of protection and the complexity of the parasite life cycle. To complicate matters, reported mechanisms of protection against the liver stage of the parasite differ not only between human and rodent malaria species, but also between different rodent malaria species. Therefore, infection of vaccinated animals with live parasites, as has previously been used to evaluate anti-malarial drugs, remains the most, if not only, meaningful readout of vaccine efficacy [2, 3]. Such a challenge model should meet the following requirements: 1) reproducible infection of a predictable proportion of the challenge cohort; 2) establishment of infection using numbers of parasites consistent with natural infection, and 3) a predictable time to patency. The most frequently used method for challenging animals with malaria is the intravenous (tail vein) injection of parasites isolated from the salivary glands of Anopheles mosquitoes. This method was first described for the Plasmodium berghei model almost four decades ago  and has not significantly evolved since. In this method, mice are injected with a defined number of sporozoites. However, the number of sporozoites required to infect 90-100% of the mice ranges from 30 to 5,000 sporozoites. This number also varies widely from day to day, from mouse strain to mouse strain and from lab to lab (personal observation and [4–7]). The significant variability may be a consequence of changes in sporozoite virulence or to host response to extraneous materials in the inoculum such as mosquito debris, salivary gland flora, or dead sporozoites . In addition, differences reported by different laboratories are presumably exacerbated by the use of laboratory-specific isolates and sub-strains of the parasite. Obtaining consistent IV infection of the frequently used BALB/c mice has been especially problematic. Scheller and colleagues approached establishing an effective challenge model by using gradient centrifugation to purify parasites . Purification of sporozoites by this method produced more reproducible infections, but also required 5,000 sporozoites per inoculum, which is far larger an amount than the 25 to 250 sporozoites estimated to be inoculated during a mosquito bite challenge [9–11].
In addition to the technical problems associated with the IV challenge model, the approach also raises very serious scientific concerns. In contrast to the IV injected parasites, Plasmodium delivered by their arthropod vector, the Anopheles mosquito, are not injected directly into the blood stream, but rather into avascular portions of the skin from where they travel into the liver over an extended period of time [11, 12]. It is unclear how this transient existence of the parasite in host tissue outside the hepatocytes affects its viability. Recent evidence suggests that a good proportion of injected sporozoites either remain close to the entry site in the dermis or reach the lymph node . It remains to be determined what the consequence of these different pathways is for mounting of a host immune response. Convincing evidence already exists that bypassing this extra-hepatic phase can lead to unacceptable conclusions regarding effector mechanism when analyzing vaccine-induced protection against liver stage infection. For instance, in one study, sporozoites delivered to the skin by a mosquito were rapidly immobilized by sporozoite-antigen specific antibodies while still in the skin . In another study where the IV challenge was used to determine the effector mechanism of a genetically-attenuated sporozoite vaccine, CD8+ T-cells were implicated in immune protection . This conclusion is likely incomplete since vaccine-induced antibodies did not have the opportunity to exert their effect as the transit time of the IV injected parasites from injection site to the liver was too short . The impact of the challenge route on the efficacy of a passive (monoclonal anti-CSP antibodies) P. berghei vaccine was also observed in a side-by-side comparison of the IV and mosquito bite challenge in the P. berghei model of CD-1 mice . The outcome of this study, however, was reversed with antibody-injected mice appearing better protected after IV challenge than mosquito bite infection. In the Plasmodium yoelii model, others were unable to obtain reliable challenge results in BALB/c mice by using varying numbers of infected Anopheles stephensi mosquitoes , which is unexpected in light of the sensitivity of this mouse strain to P. yoelii. Despite the obvious shortcomings, the IV challenge model nevertheless continues to be used for reporting malaria vaccine efficacy [18–20].
An alternative challenge approach introduced several decades ago is through the bite of an infectious mosquito, the natural delivery route of transmission . This is also the method of choice for the challenge of human volunteers in P. falciparum vaccine trials [22–25]. To date, no candidate vaccine has shown reproducible field efficacy without demonstration of efficacy in a clinical challenge trial using this approach . However, the mosquito bite challenge is rarely employed in mouse models of malaria. The primary reasons for this are that it is more labour intensive requiring more and better trained personnel, and well established conditions for a mosquito bite challenge of mice are not readily available. While the number of sporozoites delivered by a single bite of an infected mosquito may still not precisely be known [9, 10], another study using PCR to detect parasite RNA in the liver forty hours after a blood meal concluded that the inoculum from a single mosquito bite is quite consistent . These observations indicated the need for optimizing the mosquito bite challenge model to consistently deliver the same inoculum. This can be accomplished by only challenging with a single infected mosquito. Protective immunity may be overwhelmed when using the previously described bulk-challenge method  in which a pool of mosquitoes with an unknown and variable infected portion are allowed to feed.
The objective of this study was to first optimize and then compare the IV with the single mosquito bite challenge method and characterize the parameters required to reliably challenge mice. The mosquito bite challenge method described here was successfully used to determine the efficacy of the first P. berghei CSP DNA vaccine [29, 30]. The single mosquito bite challenge is clearly superior to the IV injection of isolated parasites thus confirming the conclusions of others who only used the CD-1 mouse model . However, the increased need for manpower and longer duration of a mosquito bite challenge, especially for large-scale vaccine studies represent a significant hurdle for its acceptance. Therefore, attention was focused on a compromise approach, the subcutaneous injection of isolated parasites into the inguinal site of mice [31–33]. This approach combines the targeting of the correct anatomical site for the delivery of parasites with the ease of the intravenous injection, while eliminating the need to prepare the mice for the procedure (i.e., warming them for IV injection or anesthetizing them for mosquito-bite challenge) and produces highly reproducible challenge outcomes.
Mice and parasites
Female, 4-6 wk-old, BALB/c, C57BL/6, and ICR (CD-1) mice were obtained from The Jackson Labs. CD-1 mice for the subcutaneous challenge experiments were from Harlan Sprague-Dawley. ANKA strain P. berghei parasites were maintained at the Division of Entomology (WRAIR). For needle-based challenges, parasites were isolated from mosquito salivary glands 26 to 28 days after infection without further purification.
Parasites were delivered by using a 1.0 ml tuberculin syringe and a 30 gauge needle. Sporozoites were dissected into M199 medium (GIBCO/Invitrogen) containing 5% normal BALB/c mouse serum (Harlan Bioproducts for Science Inc., Indianapolis, IN) which was standardized and pathogen screened. All further manipulations and dilutions of sporozoites were with this medium. Diluted sporozoites were maintained on ice until use within two hours. For challenge, mice were warmed via a heat lamp and injected IV with 100 μl of a sporozoite suspension containing from 10-10,000 sporozoites.
Mosquito bite challenge
Anopheles stephensi mosquitoes were placed into small, sealed, screened containers. Mice were sedated with a 0.1 ml intraperitoneal injection of a mixture containing 25 mg/ml Ketaset® (ketamine HCL, Wyeth/Pfizer, New York, NY) and 5 mg/ml Rompun® (xylazine HCL, Bayer, Pittsburgh, PA) in sterile saline. Sedated animals were placed individually on the containers until it was observed that a blood meal had been taken. The sex and number of the mosquitoes in each carton were monitored and controlled during all experimental procedures. An infectious mosquito bite was confirmed by dissection of the mosquito salivary glands and viewed by phase-contrast microscopy. If no sporozoites were observed, this process was repeated until an infected mosquito was identified.
Subcutaneous inguinal challenge
Parasites were isolated and injected as described above for IV challenge, but delivered to the subcutaneous pouch at the base of the hind leg of mice. This route was chosen because it is easily accessible and holds larger amounts of liquid than other subcutaneous sites.
Blood stage infection was determined in challenged animals by Giemsa-stained thin blood films. Thin blood films were prepared on days 7 and 14 by removing a less than 1 mm section of the distal end of the tail and spotting approximately 3 μl of blood onto a microscope slide. Slides were air dried, fixed with 100% methanol and stained with a 10% Giemsa solution for 10 minutes at room temperature. Slides were evaluated at a 1000× magnification (oil-immersion) using a Nikon E400 Eclipse microscope by reading 20 fields per slide.
Vaccination of mice with a DNA vaccine
In order to evaluate the challenge models under vaccine trial conditions, mice were vaccinated with DNA vaccines encoding the P. berghei CSP gene previously reported to protect mice against challenge [29, 31]. Briefly, a plasmid containing the full length CSP-gene of P. berghei (designated here CSP(+)) was used for the initial experiments. For subsequent independent experiments, a plasmid encoding the full length CSP without the GPI anchor sequence (designated CSP(-A)) was employed. The CSP(-A) plasmid yields increased vaccine efficacy compared to the full length CSP(+) construct . Plasmids were grown in E. coli and purified by double banding on cesium chloride gradients followed by chromatography on Qiagen columns (Valencia, CA) according to manufacturer's recommendation. DNA was precipitated on gold beads and used to vaccinate mice epidermally by gene gun delivery targeting two sites of the shaved abdominal area with 1 μg DNA dose each. When using the CSP(+) plasmids, animals were immunized two times at four-week-intervals and challenged two weeks after the last immunization. When using the CSP(-A) plasmid, mice received three immunizations at four-week intervals.
In order to achieve an 84% chance to detect a statistical difference between an infection rate of 80% (a negative control rate) and an infection rate of 10% (a non-control infection rate), using Fisher's exact test (2-sided, with alpha = 0.05), ten mice per group were required (nQuery Advisor 6.0 software, Statistical Solutions, Saugus, MA).
Challenge efficiency for IV and mosquito bite challenge
Comparison of intravenous vs. single mosquito bite challenge models
Single Mosquito Bite e)
Mouse Strains Tested
By using the single mosquito bite challenge in BALB/c mice, a mean of 98% of challenge controls were infected in at least 80% of the challenge experiments performed. In replicate experiments with C57BL/6 and ICR (CD-1) mice, 100% of naïve animals were infected 100% of the time (Table 1).
Conditions for an effective single bite challenge
Sex mixed feeding populations increase mean feeding times
Mosquito feeding population b)
Average time a)
Average time a)
1 Infected c) + 2 Uninfected Females
11.5 ± 4.3
7.7 ± 1.3
1 Infected + 1 Uninfected Female
8.7 ± 2.9
1 Infected Female + 2 Males
2.4 ± 0.8
5.4 ± 0.8
1 Infected Female + 1 Male
6.2 ± 2.9
1 Uninfected Female
2.4 ± 4.6
5.5 ± 3.2
1 Infected Female
8.7 ± 1.8
8.8 ± 2.4
Categorization of IV challenge failures
Varying IV challenge strength and its impact on reported vaccine efficacy
Inter-experimental variations of IV challenge and effect on perceived vaccine efficacy
% Infected, p b)
LD(50) ) e
Chall. w/300 SPZ c)
30, p = 0.01
% Infected, p
Chall. w/30 SPZ
70, p = 0.11
ID50 < 30
Chall. w/100 SPZ
80, p = 0.24
ID50 < 30
Chall. w/300 SPZ
80, p = 0.24
ID50 < 30
The subcutaneous challenge as an alternative to the intravenous and bite challenge model
Sporozoite titration for subcutaneous challenge
The influence of challenge conditions on perceived vaccine efficacy
Effect of IV challenge dose on perceived vaccine efficacy
Effect of challenge route on perceived vaccine efficacy
gene gun vaccination, SQ challenge
gene gun vaccination, IV challenge
IM vaccination, SQ challenge
IM vaccination, IV challenge
The immune mechanisms responsible for protecting against Plasmodium-infection or morbidity associated with chronic infection are surprisingly still not understood. This is in part due to insufficient efforts spent on the characterization of immune correlates of protection and to the fact that different mechanisms appear to be required to protect against different species of Plasmodium.
While cytotoxic T cells have been described as the main effectors protecting mice against P. yoelii infection after immunization with a CSP-based DNA vaccine , CTL appeared to be irrelevant in mice protected from P. berghei infection following immunization with a similar vaccine . In the latter study, Th2-type antibodies recognizing specific epitopes on the CS-protein correlated with protection. Because of the lack of robust surrogate markers of protection, challenging with live parasites remains the most meaningful method to determine the potential protective efficacy of a candidate vaccine for both preclinical and clinical trials.
While vaccinated human volunteers are generally challenged through the bite of infected mosquitoes, the IV challenge model remains the most commonly used approach for infecting rodents with malaria because of the relative convenience and the ability to quantitate the sporozoite inoculum delivered. However, the number of sporozoites required to reproducibly infect 90-100% varies greatly. BALB/c mice, while frequently used for malaria vaccine studies, are particularly difficult to infect reliably. This may be due to the much higher susceptibility of this strain's innate immune system to P. berghei (but not to P. yoelii), which has been known for several decades  and had been used to question the usefulness of this mouse strain for P. berghei studies . Malaria infection in general, and specific malaria-associated molecules, have been shown to trigger inflammatory responses through the stimulation of innate immune receptors [36–39]. Many such studies were, however, conducted in vitro, and while it may be questionable whether noticeable inflammatory responses are induced by these relatively small mosquito-delivered inocula, such responses can be expected to be amplified when a relatively large amount of parasite-derived and mosquito-derived debris are delivered together. Not surprisingly, such variability can also be attributed to seasonal factors that are generally not considered such as changing microbial flora delivered with the isolated sporozoites. Malaria parasites have repeatedly been found to be surprisingly susceptible to inflammation, either caused by another infection or by inflammatory mediators. The sensitivity of sporozoites to innate immune responses was shown by Nussler and colleagues 1993 who observed that irradiated P. yoelii sporozoites could produce a spontaneous intrahepatic inhibition of infection for P. berghei sporozoites that lasted up to three weeks after delivery of the last dose of irradiated P. yoelii and that this inhibition disappeared completely after one month . Similarly, activators of innate immune responses such as CpG oligonucleotides, ligands for toll-like receptors and acute phase proteins have been shown to have a significant effect on host susceptibility and resistance against sporozoite infections [40–42].
The single infectious bite challenge model was developed as an alternative to the relatively unreliable and unpredictable IV challenge method. This method does not require the inclusion of a large number of challenge control animals in each challenge experiment that need to be injected with various numbers of SPZ to be able to reliably determine the success and virulence of the challenge. This model proved to be significantly more reliable, requiring only a single P. berghei ANKA-infected mosquito to infect most or all challenge controls regardless of their genetic background. In contrast, another study reports the need for at least five mosquitoes to reliably infect 100% of CD-1 mice . Although the reason for the discrepancy is unknown, the authors of this study nevertheless conclude that the mosquito bite challenge should be used rather than IV injection of parasites to avoid artifacts. For the P. yoelii model of malaria, a recent report suggests that the IV challenge is more reliable than the infection of BALB/c mice through mosquito bite, which in the hands of these investigators required multiple infected mosquitoes . Based on theses unexpected results, the authors recommend the IV injection of sporozoites as the preferred infection method, however, ignoring the impact on perceived vaccine efficacies.
The method is, however, more labour intensive and this underscored the need for a reliable, but more efficient challenge procedure. The use of mixed-sex mosquito-feeding populations represented a significant improvement since it decreased the time required for an infected female mosquito to take a blood meal. Specifically, the addition of two male mosquitoes enhanced the feeding behaviour of the P. berghei infected female mosquito. This simple modification decreased the time required for a normal sixty- to seventy-mouse experiment to four to six hours for challenge. The observations are consistent with previous reports that male and female mosquito interactions can dramatically alter feeding behaviour [43, 44]. Therefore, a sex-linked feeding motivator (e.g. pheromone, wing beat frequency, etc) that allows infected female mosquitoes to complete their blood meal more rapidly must be present when males and females are together, likely because feeding behaviour among female mosquitoes is directly linked to egg laying .
The present study sought to determine whether a modified mosquito-bite challenge approach in which mice are exposed to a single infected mosquito could be developed as a more reliable, reproducible and more biologically relevant alternative to the routinely used IV challenge model. After establishing standard parameters required for making this model highly reliable, it became evident that despite its effectiveness the logistical hurdles involved reduce its usefulness. It is significantly more time and labour consuming than an injection-based challenge, which limits the size of challenge experiments to around one hundred mice per experiment. Therefore, a method was explored that combines the advantages of the IV and mosquito bite models, the subcutaneous injection of sporozoites, which generates highly reliable challenge results. This route, though physiologically much more relevant than the IV route, surprisingly required larger numbers of sporozoites than did the IV route, and the size of the inoculum that is required to produce one hundred percent infectivity is within a relatively narrow range. Delivering an increasing inoculum through the subcutaneous route resulted in a bell-shaped challenge curve and the drop in challenge efficacy at doses higher than 4,000-5,000 sporozoites/mouse and is likely caused by the same factors responsible for the Type 2 failure of IV challenges, namely inflammatory responses triggered by excessive amounts of stimulators of innate immune responses within the inoculum.
The intravenous injection of sporozoites generates highly variable and poorly reproducible challenge results. Confirming the concerns of others  this study also reveals that it drastically affects the perceived efficacy of a pre-erythrocytic vaccine. The single infectious-bite challenge as described here for P. berghei is the most reliable and most relevant readout method for testing the efficacy of malaria vaccines in animal models. Since it is time and labour intensive, the subcutaneous injection of isolated sporozoites at the base of the hind leg presents itself as an acceptable alternative. This method is rapid, produces highly consistent challenge results and is much more comparable to the natural route of malaria infection than the frequently used IV challenge route.
Both injection-based challenge methods require a careful titration of the inoculum in naive control mice. Such a titration is required for each IV challenge experiment to be able to judge the virulence of the inoculum and to avoid the misinterpretation of vaccination studies. However, the subcutaneous challenge route appears significantly less sensitive to the day-to-day variations in the inoculum thus allowing the use of an initially established "standard" dose.
The authors would like to thank Dr. Jeffrey Lyon, for guidance on study design, Matthew C. Seguin Howard D. Stacey and Elizabeth Duncan for their expertise and technical assistance; Dr. Imogene Schneider, Megan Dowler, Jacqulin Glass and Dr. Tatyana Savranskaya for providing infected mosquitoes and for advice and technical assistance; and Diane Cooper (NIH Library) for editing. This work was supported by the United States Army Medical Research and Materiel Command.
The authors' views are private and are not to be construed as official policy of the Department of Defense or the U.S. Army. Research was conducted in compliance with the Animal Welfare Act and other Federal statutes and regulations relating to animals and experiments involving animals and adheres to principles stated in the Guide for the Care and Use of Laboratory Animals, NRC Publication, 1996 edition. All procedures were reviewed and approved by the Institute's Animal Care and Use Committee, and performed in a facility accredited by the Association for Assessment and Accreditation of Laboratory Animal Care, International.
- Good MF: The hope but challenge for developing a vaccine that might control malaria. Eur J Immunol. 2009, 39: 939-943. 10.1002/eji.200939390.View ArticlePubMedGoogle Scholar
- Egan JE, Weber JL, Ballou WR, Hollingdale MR, Majarian WR, Gordon DM, Maloy WL, Hoffman SL, Wirtz RA, Schneider I, Woollett GR, Young JF, Hockmeyer WT: Efficacy of murine malaria sporozoite vaccines: implications for human vaccine development. Science. 1987, 236: 453-456. 10.1126/science.3551073.View ArticlePubMedGoogle Scholar
- Cox FEG: Major animal models in malarial research: rodent. Malaria: Principles and Practice of Malariology. Edited by: IA M. 1988, Edinburgh: Churchill Livingstone, 2: 1503-1544.Google Scholar
- Nussenzweig R, Herman R, Vanderberg J, Yoeli M, Most H: Studies on sporozoite-induced infections of rodent malaria. 3. The course of sporozoite-induced Plasmodium berghei in different hosts. Am J Trop Med Hyg. 1966, 15: 684-689.PubMedGoogle Scholar
- Jaffe RI, Lowell GH, Gordon DM: Differences in susceptibility among mouse strains to infection with Plasmodium berghei (ANKA clone) sporozoites and its relationship to protection by gamma-irradiated sporozoites. Am J Trop Med Hyg. 1990, 42: 309-313.PubMedGoogle Scholar
- Scheller LF, Wirtz RA, Azad AF: Susceptibility of different strains of mice to hepatic infection with Plasmodium berghei. Infect Immun. 1994, 62: 4844-4847.PubMed CentralPubMedGoogle Scholar
- Coosemans M, Wery M, Van Marck E, Timperman G: Studies on the infectivity of Plasmodium berghei sporozoites in experimental hosts. Ann Soc Belg Med Trop. 1981, 61: 349-368.PubMedGoogle Scholar
- Nussler AK, Renia L, Pasquetto V, Miltgen F, Matile H, Mazier D: In vivo induction of the nitric oxide pathway in hepatocytes after injection with irradiated malaria sporozoites, malaria blood parasites or adjuvants. Eur J Immunol. 1993, 23: 882-887. 10.1002/eji.1830230417.View ArticlePubMedGoogle Scholar
- Vanderberg JP: Plasmodium berghei: quantitation of sporozoites injected by mosquitoes feeding on a rodent host. Exp Parasitol. 1977, 42: 169-181. 10.1016/0014-4894(77)90075-3.View ArticlePubMedGoogle Scholar
- Beier JC, Davis JR, Vaughan JA, Noden BH, Beier MS: Quantitation of Plasmodium falciparum sporozoites transmitted in vitro by experimentally infected Anopheles gambiae and Anopheles stephensi. Am J Trop Med Hyg. 1991, 44: 564-570.PubMedGoogle Scholar
- Amino R, Thiberge S, Martin B, Celli S, Shorte S, Frischknecht F, Menard R: Quantitative imaging of Plasmodium transmission from mosquito to mammal. Nat Med. 2006, 12: 220-224. 10.1038/nm1350.View ArticlePubMedGoogle Scholar
- Sidjanski S, Vanderberg JP: Delayed migration of Plasmodium sporozoites from the mosquito bite site to the blood. Am J Trop Med Hyg. 1997, 57: 426-429.PubMedGoogle Scholar
- Vanderberg JP, Frevert U: Intravital microscopy demonstrating antibody-mediated immobilisation of Plasmodium berghei sporozoites injected into skin by mosquitoes. Int J Parasitol. 2004, 34: 991-996. 10.1016/j.ijpara.2004.05.005.View ArticlePubMedGoogle Scholar
- Mueller AK, Deckert M, Heiss K, Goetz K, Matuschewski K, Schluter D: Genetically attenuated Plasmodium berghei liver stages persist and elicit sterile protection primarily via CD8 T cells. Am J Pathol. 2007, 171: 107-115. 10.2353/ajpath.2007.060792.PubMed CentralView ArticlePubMedGoogle Scholar
- Vanderberg J, Mueller AK, Heiss K, Goetz K, Matuschewski K, Deckert M, Schluter D: Assessment of antibody protection against malaria sporozoites must be done by mosquito injection of sporozoites. Am J Pathol. 2007, 171: 1405-1406. 10.2353/ajpath.2007.070661.View ArticlePubMedGoogle Scholar
- Vaughan JA, Scheller LF, Wirtz RA, Azad AF: Infectivity of Plasmodium berghei sporozoites delivered by intravenous inoculation versus mosquito bite: implications for sporozoite vaccine trials. Infect Immun. 1999, 67: 4285-4289.PubMed CentralPubMedGoogle Scholar
- Conteh S, Chattopadhyay R, Anderson C, Hoffman SL: Plasmodium yoelii-Infected A. stephensi inefficiently transmit malaria compared to intravenous route. PLoS One. 2010, 5: e8947-10.1371/journal.pone.0008947.PubMed CentralView ArticlePubMedGoogle Scholar
- Jobe O, Donofrio G, Sun G, Liepinsh D, Schwenk R, Krzych U: Immunization with radiation-attenuated Plasmodium berghei sporozoites induces liver cCD8alpha+DC that activate CD8+T cells against liver-stage malaria. PLoS One. 2009, 4: e5075-10.1371/journal.pone.0005075.PubMed CentralView ArticlePubMedGoogle Scholar
- Silva-Flannery LM, Cabrera-Mora M, Dickherber M, Moreno A: Polymeric linear Peptide chimeric vaccine-induced antimalaria immunity is associated with enhanced in vitro antigen loading. Infect Immun. 2009, 77: 1798-1806. 10.1128/IAI.00470-08.PubMed CentralView ArticlePubMedGoogle Scholar
- Romero JF, Ciabattini A, Guillaume P, Frank G, Ruggiero P, Pettini E, Del Giudice G, Medaglini D, Corradin G: Intranasal administration of the synthetic polypeptide from the C-terminus of the circumsporozoite protein of Plasmodium berghei with the modified heat-labile toxin of Escherichia coli (LTK63) induces a complete protection against malaria challenge. Vaccine. 2009, 27: 1266-1271. 10.1016/j.vaccine.2008.12.010.View ArticlePubMedGoogle Scholar
- Yoeli M, Upmanis RS, Vanderberg J, Most H: Life cycle and patterns of development of Plasmodium berghei in normal and experimental hosts. Mil Med. 1966, 131 (Suppl): 900-914.PubMedGoogle Scholar
- Gordon DM, McGovern TW, Krzych U, Cohen JC, Schneider I, LaChance R, Heppner DG, Yuan G, Hollingdale M, Slaoui M, Hauser SP, Voet P, Sadoff JC, Ballou WR: Safety, immunogenicity, and efficacy of a recombinantly produced Plasmodium falciparum circumsporozoite protein-hepatitis B surface antigen subunit vaccine. J Infect Dis. 1995, 171: 1576-1585.View ArticlePubMedGoogle Scholar
- Herrington DA, Clyde DF, Davis JR, Baqar S, Murphy JR, Cortese JF, Bank RS, Nardin E, DiJohn D, Nussenzweig RS, Nussenzweig V, Torres JR, Murillo J, Cortesia M, Struchler D, Hollingdale MR, Levine M: Human studies with synthetic peptide sporozoite vaccine (NANP)3-TT and immunization with irradiated sporozoites. Bull World Health Organ. 1990, 68 (Suppl): 33-37.PubMed CentralPubMedGoogle Scholar
- Hoffman SL, Edelman R, Bryan JP, Schneider I, Davis J, Sedegah M, Gordon D, Church P, Gross M, Silverman C, Hollingdale M, Clyde D, Sztein M, Losonsky G, Paparello S, Jone TR: Safety, immunogenicity, and efficacy of a malaria sporozoite vaccine administered with monophosphoryl lipid A, cell wall skeleton of mycobacteria, and squalane as adjuvant. Am J Trop Med Hyg. 1994, 5: 603-612.Google Scholar
- Stoute JA, Slaoui M, Heppner DG, Momin P, Kester KE, Desmons P, Wellde BT, Garcon N, Krzych U, Marchand M: A preliminary evaluation of a recombinant circumsporozoite protein vaccine against Plasmodium falciparum malaria. RTS, S Malaria Vaccine Evaluation Group. N Engl J Med. 1997, 336: 86-91. 10.1056/NEJM199701093360202.View ArticlePubMedGoogle Scholar
- Moorthy VS, Diggs C, Ferro S, Good MF, Herrera S, Hill AV, Imoukhuede EB, Kumar S, Loucq C, Marsh K, Ockenhouse CF, Richie TL, Sauerwein RW: Report of a Consultation on the Optimization of Clinical Challenge Trials for Evaluation of Candidate Blood Stage Malaria Vaccines, 18-19 March 2009, Bethesda, MD, USA. Vaccine. 2009, 27: 5719-5725. 10.1016/j.vaccine.2009.07.049.View ArticlePubMedGoogle Scholar
- Bruna-Romero O, Hafalla JC, Gonzalez-Aseguinolaza G, Sano G, Tsuji M, Zavala F: Detection of malaria liver-stages in mice infected through the bite of a single Anopheles mosquito using a highly sensitive real-time PCR. Int J Parasitol. 2001, 31: 1499-1502. 10.1016/S0020-7519(01)00265-X.View ArticlePubMedGoogle Scholar
- Seguin MC, Klotz FW, Schneider I, Weir JP, Goodbary M, Slayter M, Raney JJ, Aniagolu JU, Green SJ: Induction of nitric oxide synthase protects against malaria in mice exposed to irradiated Plasmodium berghei infected mosquitoes: involvement of interferon gamma and CD8+ T cells. J Exp Med. 1994, 180: 353-358. 10.1084/jem.180.1.353.View ArticlePubMedGoogle Scholar
- Leitner WW, Seguin MC, Ballou WR, Seitz JP, Schultz AM, Sheehy MJ, Lyon JA: Immune responses induced by intramuscular or gene gun injection of protective deoxyribonucleic acid vaccines that express the circumsporozoite protein from Plasmodium berghei malaria parasites. J Immunol. 1997, 159: 6112-6119.PubMedGoogle Scholar
- Weiss R, Leitner WW, Scheiblhofer S, Chen D, Bernhaupt A, Mostbock S, Thalhamer J, Lyon JA: Genetic vaccination against malaria infection by intradermal and epidermal injections of a plasmid containing the gene encoding the Plasmodium berghei circumsporozoite protein. Infect Immun. 2000, 68: 5914-5919. 10.1128/IAI.68.10.5914-5919.2000.PubMed CentralView ArticlePubMedGoogle Scholar
- Bergmann-Leitner ES, Scheiblhofer S, Weiss R, Duncan EH, Leitner WW, Chen D, Angov E, Khan F, Williams JL, Winter DB, Thalhamer J, Lyon JA, Tsokos GC: C3d binding to the circumsporozoite protein carboxy-terminus deviates immunity against malaria. Int Immunol. 2005, 17: 245-255. 10.1093/intimm/dxh205.View ArticlePubMedGoogle Scholar
- Bergmann-Leitner ES, Duncan EH, Leitner WW, Neutzner A, Savranskaya T, Angov E, Tsokos GC: C3d-defined complement receptor-binding peptide p28 conjugated to circumsporozoite protein provides protection against Plasmodium berghei. Vaccine. 2007, 25: 7732-7736. 10.1016/j.vaccine.2007.08.030.View ArticlePubMedGoogle Scholar
- Bergmann-Leitner ES, Leitner WW, Duncan EH, Savranskaya T, Angov E: Molecular adjuvants for malaria DNA vaccines based on the modulation of host-cell apoptosis. Vaccine. 2009, 27: 5700-5708. 10.1016/j.vaccine.2009.06.059.View ArticlePubMedGoogle Scholar
- Scheiblhofer S, Chen D, Weiss R, Khan F, Mostbock S, Fegeding K, Leitner WW, Thalhamer J, Lyon JA: Removal of the circumsporozoite protein (CSP) glycosylphosphatidylinositol signal sequence from a CSP DNA vaccine enhances induction of CSP-specific Th2 type immune responses and improvesprotection against malaria infection. Eur J Immunol. 2001, 31: 692-698. 10.1002/1521-4141(200103)31:3<692::AID-IMMU692>3.0.CO;2-Y.View ArticlePubMedGoogle Scholar
- Doolan DL, Hoffman SL: IL-12 and NK cells are required for antigen-specific adaptive immunity against malaria initiated by CD8+ T cells in the Plasmodium yoelii model. J Immunol. 1999, 163: 884-892.PubMedGoogle Scholar
- Murphy JR: Host defenses in murine malaria: nonspecific resistance to Plasmodium berghei generated in response to Mycobacterium bovis infection or Corynebacterium parvum stimulation. Infect Immun. 1981, 33: 199-211.PubMed CentralPubMedGoogle Scholar
- Furuta T, Imajo-Ohmi S, Fukuda H, Kano S, Miyake K, Watanabe N: Mast cell-mediated immune responses through IgE antibody and Toll-like receptor 4 by malarial peroxiredoxin. Eur J Immunol. 2008, 38: 1341-1350. 10.1002/eji.200738059.View ArticlePubMedGoogle Scholar
- McCall MB, Netea MG, Hermsen CC, Jansen T, Jacobs L, Golenbock D, Ven van der AJ, Sauerwein RW: Plasmodium falciparum infection causes proinflammatory priming of human TLR responses. J Immunol. 2007, 179: 162-171.View ArticlePubMedGoogle Scholar
- Gowda DC: TLR-mediated cell signaling by malaria GPIs. Trends Parasitol. 2007, 23: 596-604. 10.1016/j.pt.2007.09.003.View ArticlePubMedGoogle Scholar
- Chen J, Xu W, Zhou T, Ding Y, Duan J, Huang F: Inhibitory role of toll-like receptors agonists in Plasmodium yoelii liver stage development. Parasite Immunol. 2009, 31: 466-473. 10.1111/j.1365-3024.2009.01126.x.View ArticlePubMedGoogle Scholar
- Gramzinski RA, Doolan DL, Sedegah M, Davis HL, Krieg AM, Hoffman SL: Interleukin-12- and gamma interferon-dependent protection against malaria conferred by CpG oligodeoxynucleotide in mice. Infect Immun. 2001, 69: 1643-1649. 10.1128/IAI.69.3.1643-1649.2001.PubMed CentralView ArticlePubMedGoogle Scholar
- Pied S, Tabone MD, Chatellier G, Marussig M, Jardel C, Nosten F, Mazier D: Non specific resistance against malaria pre-erythrocytic stages: involvement of acute phase proteins. Parasite. 1995, 2: 263-268.View ArticlePubMedGoogle Scholar
- Eiras AE, Jepson PC: Responses of female Aedes aegypti to host odours and convection currents using an olfectometer bioassay. Bull Entomol Res. 1994, 84207-84211.Google Scholar
- Klowden MJ: Blood, sex and the mosquito: the mechanisms that control mosquito blood-feeding behavior. BioScience. 1995, 45: 326-331. 10.2307/1312493.View ArticleGoogle Scholar
- Harwood RF, James MT: Mosquitoes. Entomology in human and animal health. 1979, New York: Macmillan Publishing Co. Inc, 169-233. 7Google Scholar
- Reed LJ, Muench H: A simple method of estimating fifty percent endpoints. Am J Hyg. 1938, 27: 493-497.Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.