Acta Leidensia最新文献

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V-NOW! Symposium on genetic variation of malaria parasites: implications for selection of adequate control strategies. Leiden, The Netherlands, November 14-16, 1990. V-NOW !疟疾寄生虫遗传变异专题讨论会:对选择适当控制策略的影响。1990年11月14日至16日,荷兰莱顿。
Acta Leidensia Pub Date : 1991-01-01
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引用次数: 0
Possible mechanisms for the maintenance of polymorphisms in Plasmodium populations. 疟原虫种群中多态性维持的可能机制。
Acta Leidensia Pub Date : 1991-01-01
D E Arnot
{"title":"Possible mechanisms for the maintenance of polymorphisms in Plasmodium populations.","authors":"D E Arnot","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>There are two views on the origin and maintenance of the high levels of polymorphism found in antigenic Plasmodium proteins. Immune selectionists consider that mutations which avoid stimulating a host response are frequent and advantageous. Proponents of the random genetic drift of selectively equivalent mutations hold that Plasmodium antigens are relatively unconstrained and can tolerate considerable structural diversity. Both sides agree that antigenic diversity is advantageous although selectionists see benefits in individual mutations whereas the proponents of random genetic drift see the advantage in the parasite's capacity to tolerate diversity per se.</p>","PeriodicalId":7108,"journal":{"name":"Acta Leidensia","volume":"60 1","pages":"29-35"},"PeriodicalIF":0.0,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12889591","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Malaria control during the nineties: what is to be expected? 九十年代的疟疾控制:可以期待什么?
Acta Leidensia Pub Date : 1991-01-01
H J van der Kaay
{"title":"Malaria control during the nineties: what is to be expected?","authors":"H J van der Kaay","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":7108,"journal":{"name":"Acta Leidensia","volume":"60 1","pages":"191-206"},"PeriodicalIF":0.0,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12983779","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Antigenic diversity in Plasmodium falciparum. 恶性疟原虫抗原多样性研究。
Acta Leidensia Pub Date : 1991-01-01
R F Anders
{"title":"Antigenic diversity in Plasmodium falciparum.","authors":"R F Anders","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>There are several mechanisms responsible for the extensive antigenic diversity found in the asexual blood stages of Plasmodium falciparum. Failure to express antigens is a feature of many isolates cultured in vitro but probably is not a major cause of antigenic diversity in vivo. Numerous point mutations occur in allelic forms of asexual blood stage antigens and are assumed to contribute to antigenic diversity but as yet few such mutations have been mapped to antigenic epitopes. A major cause of antigenic diversity is the expression of different repetitive sequences in allelic forms of several antigens including the S-antigen and the two merozoite surface antigens, MSA-1 and MSA-2. The sequencing data indicates that S-antigen genes fall into many allelic families whereas both MSA-1 and MSA-2 are dimorphic. Further diversity has arisen as a result of intragenic recombinations between the dimorphic forms of both MSA-1 and MSA-2. In addition to this diversity reflecting the expression of different allelic genes, asexual blood stages of malaria parasites undergo antigenic variation in that clonal parasite populations can vary the form of an antigen on the surface of infected erythrocytes. Antibodies or DNA probes directed against variable repeat sequences can be used to distinguish different isolates of P. falciparum. The use of antibodies to S-antigen repeats has been particularly useful for typing the parasites causing infections. The application of S-antigen typing to field studies in Papua New Guinea has demonstrated marked diversity in the parasites causing infections in one area.</p>","PeriodicalId":7108,"journal":{"name":"Acta Leidensia","volume":"60 1","pages":"57-67"},"PeriodicalIF":0.0,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12983784","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Protective immune responses as indicators of antigenic diversity and stability. 保护性免疫反应作为抗原多样性和稳定性的指标。
Acta Leidensia Pub Date : 1991-01-01
K N Brown
{"title":"Protective immune responses as indicators of antigenic diversity and stability.","authors":"K N Brown","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>By definition, the biology of a living organism must be characterized before its molecular biology can be interpreted. Malariologists are fortunate in that the malaria parasite was used as a well-controlled therapy for tens of thousands of hospital patients. During many of these treatments the opportunity was taken to study malaria and the behaviour of the parasite in detail. From these, and similar studies on volunteers, together with numerous epidemiological surveys, the operational characteristics of immunity to malaria in man have been well defined. Unfortunately this information, which exists in some detail in the older literature, does not seem to have been available to many investigators. This situation has led to interpretations of molecular data which are inconsistent with the known biology of the parasites and human-parasite relationships. This article considers how the structure of one of the best studied antigens, MSP1, can be viewed in the context of the host-parasite relationship. It postulates some testable hypotheses which aim to reconcile the molecular characteristics of the antigen with the biology and immunology of the asexual erythrocytic stage of the parasite.</p>","PeriodicalId":7108,"journal":{"name":"Acta Leidensia","volume":"60 1","pages":"111-9"},"PeriodicalIF":0.0,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12983767","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The need for live parasites for long-term immunity in malaria. 疟疾长期免疫需要活寄生虫。
Acta Leidensia Pub Date : 1991-01-01
W M Eling, C Celluzzi, C C Hermsen, T van de Wiel, J Curfs, P L Liem
{"title":"The need for live parasites for long-term immunity in malaria.","authors":"W M Eling,&nbsp;C Celluzzi,&nbsp;C C Hermsen,&nbsp;T van de Wiel,&nbsp;J Curfs,&nbsp;P L Liem","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>All of the results of the various experiments support a role for living, proliferating parasites in the efficient induction of anti-parasitic as well as anti-disease (CM) immunity. Non-proliferating parasites or material from disrupted parasites are poor or non-antigens in this respect. Three possibilities as to why living parasites are important in immunity could be considered: 1. circulating parasites contain insufficient antigen to induce protective immunity, but sufficient antigen can be produced during proliferation; 2. only circulating parasites arrive at critical places (e.g. parts of the white pulp of the spleen) for the presentation of the important antigen or induction of appropriate signals. 3. Architectural changes are needed (i.e. formation of barrie-cell-complexes) for the immune response to be effective. The first possibility explains why exoantigens, as well as live, proliferating parasites are efficient inducers of anti-CM immunity. Since these immunizations have no effect on parasitemia, additional/other immune reaction(s) are needed for anti-parasitic immunity. The important role of the spleen in malaria and malaria immunity is well-known. The second possibility includes the idea that live, proliferating parasites circulate through the spleen continuously where unsatisfactory or infected erythrocytes are removed rather than in the liver. Injected killed parasites or material from them when present in the circulation is to a larger extent taken up by the Kupffer cells from the liver rather than the spleen. Presence and uptake of parasites in the spleen may provide the critical confrontation and/or delivery of signals necessary for the development of immunity.(ABSTRACT TRUNCATED AT 250 WORDS)</p>","PeriodicalId":7108,"journal":{"name":"Acta Leidensia","volume":"60 1","pages":"167-75"},"PeriodicalIF":0.0,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12983775","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A live attenuated malaria vaccine: science or fiction? 减毒疟疾活疫苗:科学还是虚构?
Acta Leidensia Pub Date : 1991-01-01
B Mons
{"title":"A live attenuated malaria vaccine: science or fiction?","authors":"B Mons","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":7108,"journal":{"name":"Acta Leidensia","volume":"60 1","pages":"181-90"},"PeriodicalIF":0.0,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12983777","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Conserved polypeptides of Plasmodium falciparum as malaria vaccine candidates? 恶性疟原虫保守多肽作为疟疾候选疫苗?
Acta Leidensia Pub Date : 1991-01-01
S Herrera, M A Herrera, C Clavijo, A Corredor, U Certa
{"title":"Conserved polypeptides of Plasmodium falciparum as malaria vaccine candidates?","authors":"S Herrera,&nbsp;M A Herrera,&nbsp;C Clavijo,&nbsp;A Corredor,&nbsp;U Certa","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":7108,"journal":{"name":"Acta Leidensia","volume":"60 1","pages":"107-10"},"PeriodicalIF":0.0,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12982455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The pfmdr gene homologues of Plasmodium falciparum. 恶性疟原虫pfmdr基因同源物。
Acta Leidensia Pub Date : 1991-01-01
A F Cowman, S R Karcz
{"title":"The pfmdr gene homologues of Plasmodium falciparum.","authors":"A F Cowman,&nbsp;S R Karcz","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Chloroquine resistance in Plasmodium falciparum bears a striking similarity to the multi-drug resistance (MDR) phenotype of mammalian tumour cells which is mediated by P-glycoprotein. P. falciparum has two mdr-like genes (pfmdr 1 and pfmdr 2) and pfmdr 1 has been linked to the chloroquine resistance phenotype. We show that pfmdr 1 encodes a protein of 160,000 Daltons that is expressed at higher levels in a chloroquine resistant cloned isolate. The pfmdr 2 gene is located on chromosome 14 and it is in equal copy number in chloroquine resistant and sensitive isolates. Therefore amplification of pfmdr 2 is not linked to chloroquine resistance. This is in contrast to the pfmdr 1 gene which has been shown to be amplified in some chloroquine resistant isolates.</p>","PeriodicalId":7108,"journal":{"name":"Acta Leidensia","volume":"60 1","pages":"121-9"},"PeriodicalIF":0.0,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12983768","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Is Plasmodium falciparum aldolase useful for rational drug design? 恶性疟原虫醛缩酶对合理的药物设计有用吗?
Acta Leidensia Pub Date : 1991-01-01
H Döbeli, C Itin, B Meier, U Certa
{"title":"Is Plasmodium falciparum aldolase useful for rational drug design?","authors":"H Döbeli,&nbsp;C Itin,&nbsp;B Meier,&nbsp;U Certa","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>P. falciparum lacks a functional citric acid cycle. Unlike most tissues of the mammalian host, it is totally dependent on glycolysis for energy generation. A compound which selectively inhibits the parasite's ATP-generating machinery is therefore a potential antimalarial agent. Such a drug may interact in two ways: a) by inhibiting the activity of an enzyme or b) by disturbing the micro-organization of consecutive enzymes in a metabolic pathway. In mammalian tissues the glycolytic pathway involves the cytoskeleton as a matrix to keep phosphofructokinase, aldolase and glyceraldehyde-3-phosphate dehydrogenase in an optimal sterical position for rapid substrate conversion. For instance, these three enzymes bind to the band 3 protein in erythrocytes or to actin in muscle cells. P. falciparum aldolase binds with very high affinity to the band 3 protein of human erythrocyte ghosts. However, the true in vivo site of association is believed to be actin II of P. falciparum. This actin has a sequence element which is almost identical to that of the band 3 aldolase binding site. We therefore suppose that plasmodia exploit a similar matrix organization. If true, the association of these enzymes with the cytoskeleton is a target for novel antimalarials. In contrast to all vertebrate aldolases, P. falciparum and P. berghei aldolases have two neighbouring lysine residues near the carboxy-terminus. We show here that mutagenesis of these basic residues has an effect on the catalytic constants Vmax and KM and moreover, the ability to bind to band 3 is reduced.(ABSTRACT TRUNCATED AT 250 WORDS)</p>","PeriodicalId":7108,"journal":{"name":"Acta Leidensia","volume":"60 1","pages":"135-40"},"PeriodicalIF":0.0,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12983771","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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