Induction of multiple anti-c-erbB-2 specificities accompanies a classical idiotypic cascade following 2B1 bispecific monoclonal antibody treatment

 The bispecific monoclonal antibody (bsmAb) 2B1, targeting the extracellular domain of c-erbB-2, the protein product of the HER-2/neu proto-oncogene, and FcγRIII (CD16), expressed by human natural killer cells, neutrophils and differentiated monocytes, mediates the specific cytotoxic activity of these effector cells to tumor cells. A group of 24 patients with c-erbB-2-overexpressing tumors were treated with intravenously administered 2B1 in a phase I clinical trial and followed after treatment to evaluate the diversity and extent of the 2B1-induced humoral immune responses. As expected, 17 of 24 patients developed human anti-(murine Ig) antibodies (HAMA) to whole 2B1 IgG in a range from 100 ng/ml to more than 50 000 ng/ml; 10 of these patients (42%) had strong (at least 1000 ng/ml) HAMA responses, some of which were still detectable at day 191. These responses were usually associated with similar reactivity to the F(ab′)₂ fragments of the parental antibodies 520C9 (anti-c-erbB-2) and 3G8 (anti-CD16). We sought evidence of an idiotypic cascade induction, indicating a prolonged specific treatment-induced effect on at least one selected target of 2B1. Using competition-based enzyme-linked immunosorbent assays, specific anti-idiotypic antibodies (Ab2) were detectable against 520C9 in 11 patients and against 3G8 in 13 patients. Peak anti-idiotypic antibodies generally occurred 3–5 weeks from treatment initiation, with a downward trend thereafter. There was a statistically significant correlation among the induction of significant HAMA responses, anti-idiotypic antibody production and the development of antibodies to c-erbB-2. The anti-c-erbB-2 responses, which were distinct from anti-anti-idiotypic (Ab3) antibodies, were detected in the post-treatment sera of 6/16 patients examined. No obvious correlation could be made between the development of humoral immune responses, the dose received, and the clinical response. Future investigations involving 2B1 therapy will concentrate on investigating an association of these humoral responses to any c-erbB-2-specific cellular responses. Manipulations of 2B1 therapy effects that augment immunity to c-erbB-2 could provide additional avenues for immunotherapy with this and other bispecific antibodies. Received: 1 August 1996 / Accepted: 28 March 1997     

Glycans as targets for monoclonal antibodies that protect rats against Trichinella spiralis

We have investigated the role of glycans on Trichinella spiralisantigens in recognition by rat monoclonal antibodies (mAbs)which protect rat pups against challenge with the parasite.In pups born to infected dams or pups passively immunized withmAbs, antibodies eliminate a challenge dose from the intestinewithin hours (‘rapid expulsion’). Because such dramaticprotection can be afforded by mAbs, we have sought to characterizethe parasite antigens they target In this report we show thatprotective antibodies were unable to bind excretory/secretory(ES) antigens de-glycosylated with trifluoromethanesulphonicacid (TFMS). In addition, oligosaccharides isolated from glycoproteinsby alkaline hydrolysis or peptlde: Nglycosidase F (PNGase F)digestion were bound by protective, but not non-protective,mAbs. Glycans affinity purified with protective mAb 9D boundto all but one protective mAb. These antibodies have been shownpreviously to bind to the surfaces of intact larvae, indicatingthat the glycan is exposed on the parasite surface. Candidateglycans that may be involved in binding protective mAbs haveunusual tri- and tetra-antennary structures with terminal tyvelosemoieties (Reason et al., Glycobiology, 4, 000-000, 1994). Coatingof the larval surface with such glycans may serve to protectthe parasite and its secreted products from enzymatic attackas the parasite travels to and resides in its epithelial niche. glycans protective antibodies Trichinella spiralis     

Novel and functional regulatory SNPs in the promoter region of <Emphasis Type="Italic">FOXP3</Emphasis> gene in a Gabonese population

Parasites exert a selection pressure on their hosts and are accountable for driving diversity within gene families and immune gene polymorphisms in a host population. The overwhelming response of regulatory T cells during infectious challenges directs the host immune system to lose the ability to mount parasite specific T cell responses. The underlying idea of this study is that regulatory single nucleotide polymorphism (SNPs) can cause significant changes in gene expression in functional immune genes. We identified and investigated regulatory SNPs in the promoter region of the FOXP3 gene in a group of Gabonese individuals exposed to a variety of parasitic infections. We identified two novel and one promoter variants in 40 individual subjects. We further validated these promoter variants for their allelic gene expression using transient transfection assays. Two promoter variants, −794 (C/G) and the other variant −734/−540 (C/T) revealed a significant higher expression of the reporter gene at basal level in comparison to the major allele. The identification of SNPs that modify function in the promoter regions could provide a basis for studying parasite susceptibility in association studies.     

Terminal {beta}-linked tyvelose creates unique epitopes in Trichinella spiralis glycan antigens

Indirect evidence that the immunodominant N-glycans of the parasite,Trichinella spiralis are capped by novel ß-linked3,6-dideoxy-D-arabinohexopyranosyl residues (tyvelase, Tyv)was obtained from immunochemical assays employing monoclonalantibodies and synthetic oligosaccharides. Three of four previouslycharacterized monoclonal antibodies generated from the lymphocytesof T.spiralis infected rats bind BSA glycoconjugates bearingthe synthetic epitope ß-D-Tyvp(1     

Retinoids modulate P2U purinergic receptor-mediated changes in transcervical paracellular permeability

In human cervical cells, extracellular ATP induces an acutedecrease in the resistance of the lateral intercellular space, thephase I response, followed by adelayed increase in tight junctional resistance, thephase II response. These responses depend on vitamin A because incubation of cells in retinoid-free medium(RFM) abolished both responses. Treatment with retinoic acid restoredthe phase I response in full, but theamplitude of the phase II response wasrestored only partly. Shorter incubations and lower concentrations ofretinoic acid [half-maximal effective concentration(K_1/2) = 0.1 µM] were required for restoring the phaseI response than were required for reversing thephase II response(K_1/2 = 1 µM).The phase I response could be restoredby ligands that bind to either retinoic acid receptors (RARs) orretinoid X receptors, but only RAR agonists had an effect onphase II response. RFM had no effecton decreases in resistance induced by ionomycin, but it attenuatedphase II-like increases in resistanceinduced by KCl or by1,2-dioctanoyl-sn-diglycerol (diC8).Actinomycin D blocked phase IIresponse but not phase I response orthe responses to ionomycin, KCl, or diC8. These results suggest thatretinoids act on cervical cells via distinct retinoid receptormechanisms and modulate phase I andphase II changes in resistance byregulating distinct signal mechanisms.

     

Cerebral amyloid plaques in Alzheimer’s disease but not in scrapie-affected mice are closely associated with a local inflammatory process

Complement proteins of the classical pathway can be immunohistochemically identified in cerebral amyloid plaques in Alzheimer’s disease. Microglial cells in and around amyloid plaques express class II major histocompatibility (MHC) antigens and complement receptors CR3 and CR4. Negative immunostaining for immunoglobulins and for T-cell subsets in the brain parenchyma demonstrates a lack of evidence for the involvement of specific immune responses (such as an immune complex-mediated complement activation or a cell-mediated immune response) in cerebral amyloid deposits in Alzheimer’s disease. Cerebral amyloid plaques in scrapie-affected mice (slow-virus induced encephalopathy) do not contain complement factors C1q and C3c and are not clustered with microglial cells expressing MHC class II molecules or complement receptor CR3. The data presented suggest the induction of a reactive inflammatory process by β/A4 amyloid in the human brain, but not by scrapie-induced PrP amyloid in mice. Our findings do not support the hypothesis that the immune system is involved in the generation of amyloid plaques in Alzheimer’s disease. This study was partly supported by a grant from the Praeventiefonds, project 28–1945     

卵形鲳鲹对刺激隐核虫的免疫应答和免疫保护研究

用刺激隐核虫（Cryptocaryon irritans）的幼虫对卵形鲳鲹（Trachinotus ovatus）进行腹腔注射和体表感染,然后每隔1周用阻动试验（Immobilization assay）检测免疫鱼的抗血清和皮肤培养液对激刺隐核虫幼虫的阻动效价,在第14周,分别用亚致死剂量和致死剂量的刺激隐核虫幼虫对免疫鱼攻毒以检测所产生的免疫保护力。实验结果显示：两种免疫方法都能让卵形鲳鲹的血清和皮肤生成阻动刺激隐核虫幼虫的特异性抗体,并能使被免疫鱼获得明显的免疫保护,但是体表感染免疫组的血清和皮肤培养液的阻动效价都要比腹腔注射免疫组高,所获得的免疫保护力也更强。同时还发现,免疫鱼血清和皮肤培养液中的抗体存在明显的差异：两者的最初生成时间、达到峰值的时间、变化规律以及阻动效价等都不一致。因此,我们推测鱼类的系统免疫应答和皮肤粘膜免疫应答有可能是相互独立的,或者是不同步的。鱼类的体液免疫应答,特别是粘膜免疫应答对抵御刺激隐核虫的感染起了重要的作用,采用刺激隐核虫虫体疫苗可能成为预防海水鱼类白点病的一种选择。     

Ultrastructural Aspects of Graft Incompatibility Between Pear and Quince In vitro

Callus cells of pear (Pyrus communis cv. ‘Bartlett’)underwent lethal cellular senescence in response to graftingwith callus cells of quince (Cydonia oblonga cv. ‘VanDeman’). Similar responses occurred when the cells werein direct contact and when they were separated by a porous membranefilter. These results indicate that direct cellular contactis not necessary to elicit graft incompatibility between pearand quince. Cydonia oblonga, grafting, incompatibility, pear, Pyrus communis, quince     

Peptide epitope mapping in vaccine development: Introduction

Protection from infectious disease by the host immune response requires specific molecular recognition of unique antigenic determinants of a given pathogen. An epitope is an antigenic determinant which: 1) specifically stimulates the immune response (either B or T cell mediated); and 2) is acted upon by the products of these protective mechanisms. In B cell immunity, antibodies produced from stimulation by specific epitopes recognize and bind to these same antigenic structures. Identification of protective epitopes is extremely valuable to successful vaccine development. In order to be protective these antibodies must, in addition to recognition and binding, interfere with some vital step in pathogenesis such as adherence or toxin action. Protein B cell epitopes are frequently composed of the side chains (R-groups) of the amino acids found at solvent-exposed surfaces. These epitopes are classified as continuous (also linear or sequential) if composed of a single antibody-recognizing element located at a single locus of the primary structure. They are discontinuous (or assembled) if more than one physically separated entity is involved. T cell epitopes are peptides on the surface of antigen-presenting cells (macrophages, dendritic cells, and B cells) that are bound to major histocompatibility proteins; the T cell recognizes this peptide-MHC complex. Received 12 August 1996/ Accepted in revised form 03 November 1996     

The right response at the right time: Exploring helminth immune modulation in sticklebacks by experimental coinfection

Parasites are one of the strongest selective agents in nature. They select for hosts that evolve counter‐adaptive strategies to cope with infection. Helminth parasites are special because they can modulate their hosts’ immune responses. This phenomenon is important in epidemiological contexts, where coinfections may be affected. How different types of hosts and helminths interact with each other is insufficiently investigated. We used the three‐spined stickleback (Gasterosteus aculeatus) – Schistocephalus solidus model to study mechanisms and temporal components of helminth immune modulation. Sticklebacks from two contrasting populations with either high resistance (HR) or low resistance (LR) against S. solidus, were individually exposed to S. solidus strains with characteristically high growth (HG) or low growth (LG) in G. aculeatus. We determined the susceptibility to another parasite, the eye fluke Diplostomum pseudospathaceum, and the expression of 23 key immune genes at three time points after S. solidus infection. D. pseudospathaceum infection rates and the gene expression responses depended on host and S. solidus type and changed over time. Whereas the effect of S. solidus type was not significant after three weeks, T regulatory responses and complement components were upregulated at later time points if hosts were infected with HG S. solidus. HR hosts showed a well orchestrated immune response, which was absent in LR hosts. Our results emphasize the role of regulatory T cells and the timing of specific immune responses during helminth infections. This study elucidates the importance to consider different coevolutionary trajectories and ecologies when studying host‐parasite interactions.     

Cyclops predation on ciliates: species.specific differences and functional responses

Experiments were conducted to measure to what extent cyclopoidcopepods ingest ciliated protists. Five freshwater ciliate species,ranging in size from 22 to 120 µm diameter, were testedwith two species of cyclopoids: Cyclops abyssorum and Cyclopskolensis. Ingestion rates were measured by radiolabeling ciliateswith ¹⁴C, and from these, functional response curves (the changein ingestion rate with changing cell densities) were constructed.Cyclopoids ingest ciliates with very high estimated maximalrates of >200 cells cyclopoid^–1 h^–1 However,there are large differences in ingestion rates that are notpredictable by the size of predator or prey. One ciliate speciesof intermediate size, Coleps hirtus, is nearly immune from cyclopoidpredation at all measured ciliate densities. Three other smallciliate species that move in rapid jumps elicit Honing type3 functional responses, with very little change in ingestionrates at low ciliate densities. Thus, while cyclopoids are capableof having a very considerable impact on ciliate populations,some ciliate species appear to have behavioral, morphologicalor chemical defenses to reduce their vulnerability. This callsinto question the practice of considering ciliates a homogeneousgroup when constructing food web models.     

Flowering Responses of Contrasting Ecotypes of Poa annua and their Putative Ancestors Poa infirma andPoa supina

Flowering responses of two Australian and six Norwegian populationsof Poa annua and their putative ancestors P. infirma and P.supina were studied in controlled environments. The two Australianpopulations originating from suburban parks in Canberra hadopposite daylength flowering responses across the range of temperaturestested (9–21 °C), one being a quantitative short-day(SD) plant with no response to vernalization, the other a quantitativelong-day (LD) plant with a quantitative vernalization requirement(winter annual type). Variation in earliness of flowering withinthe former population was shown to be genetically determined,and testing of selfed progenies indicated that the populationis an aggregate of several largely homozygous lines with divergentflowering responses. Two lowland populations from southern Norwaywere both quantitative LD plants with no vernalization response,while two alpine snowbed populations from southern Norway andtwo high-latitude, subarctic populations from northern Norwaywere quantitative SD plants with an obligatory plant vernalizationor SD requirement for flowering. Two populations of P. supinaexhibited the same flowering responses as the alpine and high-latitudepopulations of P. annua with an obligatory plant vernalizationor SD requirement for flowering. A combination of SD and lowtemperature (9–12 °C) for 8–10 weeks was optimalfor induction and inflorescence initiation. On the other hand,P. infirma was found to be an early-flowering quantitative SDplant which flowered freely across the range of temperatures(9–21 °C) as a typical summer annual. The experimentsdemonstrate that virtually any kind of photoperiodic and vernalizationresponses can be found among populations of P. annua. Theseversatile flowering responses reflect the contrasting floweringresponses of P. supina and P. infirma, and add strong supportto the hypothesis that P. annua has originated from these species.Copyright 2001 Annals of Botany Company Adaptation, evolution, flowering, Poa annua, P. infirma, P. supina, photoperiod, vernalization     

Approaches towards DNA Vaccination against a Skin Ciliate Parasite in Fish

Rainbow trout (Oncorhynchus mykiss) were immunized with plasmid DNA vaccine constructs encoding selected antigens from the parasite Ichthyophthirius multifiliis. Two immobilization antigens (I-ags) and one cysteine protease were tested as genetic vaccine antigen candidates. Antigenicity was evaluated by immunostaining of transfected fish cells using I-ag specific mono- and polyclonal antibodies. I. multifiliis specific antibody production, regulation of immune-relevant genes and/or protection in terms of parasite burden or mortality was measured to evaluate the induced immune response in vaccinated fish. Apart from intramuscular injection, needle free injection and gene gun delivery were tested as alternative administration techniques. For the I-ags the complement protein fragment C3d and the termini of the viral haemorrhagic septicaemia virus glyco(G)protein (VHSV G) were tested as opsonisation and cellular localisation mediators, respectively, while the full length viral G protein was tested as molecular adjuvant. Expression of I-ags in transfected fish cells was demonstrated for several constructs and by immunohistochemistry it was possible to detect expression of a secreted form of the Iag52B in the muscle cells of injected fish. Up-regulations of mRNA coding for IgM, MHC I, MHC II and TCR β, respectively, were observed in muscle tissue at the injection site in selected trials. In the spleen up-regulations were found for IFN-γ and IL-10. The highest up-regulations were seen following co-administration of I-ag and cysteine protease plasmid constructs. This correlated with a slight elevation of an I. multifiliis specific antibody response. However, in spite of detectable antigen expression and immune reactions, none of the tested vaccination strategies provided significant protection. This might suggest an insufficiency of DNA vaccination alone to trigger protective mechanisms against I. multifiliis or that other or additional parasite antigens are required for such a vaccine to be successful.     

Humoral immune responses of channel catfish (Ictalurus punctatus) fry and fingerlings exposed toEdwardsiella ictaluri

The ability of channel catfish to develop antibody responses to Edwardsiella ictaluri was evaluated. Fish were produced and reared under specific pathogen free (SPF) conditions. At the ages of 1, 2, 3 and 4 weeks and 2, 3, 4, 5, and 6 months post-hatch, a group of these naive fish were given a primary immersion exposure to E. ictaluri (mean doses of 6·4×10⁴ cfu ml⁻¹of tank water). Each group received a secondary immersion exposure 4 weeks after the primary exposure and were sampled 2 weeks after each exposure. Control groups were exposed to sterile culture medium. Specific antibody titres were first detected in fish exposed at 4 weeks post-hatch at an average weight of 85 mg. A secondary response was first demonstrated by fry that received a primary exposure at 4 weeks post-hatch and a secondary exposure at 8 weeks post-hatch. However, a true boosting effect was first demonstrated in fish that received their primary exposure at 2 months of age. Fish given a primary exposure before 4 weeks of age and a secondary exposure failed to produce a significant antibody response, even though they were the same age at secondary exposure as fish that produced strong antibody responses upon primary exposure. This phenomenon suggests that immunological tolerance was induced and indicates that channel catfish may not be capable of generating a humoral immune response before four weeks of age.     

Simultaneous changes in cell quotas of microcystin, chlorophyll a, protein and carbohydrate during different growth phases of a batch culture experiment with Microcystis aeruginosa

The cell quotas of microcystin (Q_mcyst), protein (Q_prot), chlorophylla (Q_chloro) and carbohydrate (Q_carbo), as well as the net productionrates of these parameters, were determined during the exponentialand stationary phases in nine batch cultures of Microcystisaeruginosa (CYA 228) at light regimes from 33 to 53 µmolphotons m^–2 s^–1. The following results were obtained.(i) A parallel pattern was found in the changes of Q_mcyst, Q_prot,Q_chloro and Q_carbo during the entire growth cycle and significantcorrelations were recorded between Q_mcyst and Q_prot, Q_chloroand Q_carbo. (ii) The net microcystin production rate (µ_mcyst)was positively correlated with the specific cell division rate(µ_c), the chlorophyll production rate (µ_chloro)and the protein production rate. (iii) A significant inverselinear relationship was found between µ_c and Q_mcyst, i.e.cultures with a positive µ_c had a Q_mcyst between 110 and400 fg microcystin cell^–1, while declining cultures hadQ_mcyst values >400 fg microcystin cell^–1. Maximum variationin Q_mcyst within cultures was 3.5-fold. Collectively, the resultsshow that cells produced microcystin at rates approximatingthose needed to replace losses to daughter cells during divisionand that microcystin was produced in a similar way to proteinand chlorophyll, indicating a constitutive microcystin production.     

Structure and Development of the Primary Haustorium in Alectra vogelii Benth. (Scrophulariaceae)

Anatomical observations were made on the structure and developmentof the primary haustorium of Alectra vogelii. Its developmentinvolves a mutual aggressive growth of both the host and parasitetissues resulting in the formation of a very large and complextuberous organ. One of the host tissues whose growth is stimulatedby parasite infection is the pericycle whose cells divide repeatedlyand grow around and within the parasite haustorial cortex. Fromvarious points of the proliferating host pericycle, roots becomeinitiated and eventually the entire surface of the haustoriumbecomes covered with these roots. We have referred to them as‘haustorial roots’, a term which we have re-examinedand redefined. True xylary connections are established not onlybetween the parasite and the host root but also between theparasite and these ‘haustorial roots’. The uniquedevelopment of primary haustorium and ‘haustorial roots’in A. vogelii is discussed in relation to the development ofprimary haustoria in other root parasites.     

Dunaliella salina: A model System for Studying the Response of Plant Cells to Stress

This review focuses on the biochemical and physiological responseof the halotolerant green alga, Dunaliella salina, to conditionsof stress. It is now well established that in response to stress,cells of Dunaliella salina var. bardawil show increased glycerolproduction, massive ßcarotene accumulation and enhancedabscisic acid metabolism. In this respect, cellular responsesare regulatory and seem to depend on a diversity of mechanismswhich may be linked to a modification of the abscisic acid balance.Dunaliella lacks a rigid cell wall and the cellular contentsare enclosed by an elastic plasma membrane that permits rapidcell volume changes in response to extracellular changes inosmolarity. Based on the ‘stretch activated ion channelsmodel’ reviewed recently by Kirst (1990) we propose thefollowing cascade of responses: volume change/distortion ofplasmalemma     

Photosynthesis in the Tapinanthus-Diplorhynchus Mistletoe-Host Relationship

Hill reaction activity and gas exchange were studied in thesouthern African mistletoe Tapinanthus vittatus, its host treeDiplorhynchus condylocarpon and uninfected trees of the samespecies. Photosynthetic potential was assessed by measuringHill reaction activities in isolated thylakoids: reaction ratesin the parasite were less than half those of the host or uninfectedtrees. In addition, parasite thylakoids were more sensitiveto heat treatment than those of the trees. Mean maximum CO₂assimilation rates (±s.e.) were significantly lower (4·2±0·24µmol m^-1 s^-1) in the parasite, compared to both uninfectedtrees (7·6±0·22), and those of the infectedhost (5·2±0·27). Chlorophyll contents (±s.e.)were 800±40 mg m^-2 in the parasite, lower in uninfectedtrees (490±80) and lowest in infected trees (310±70).CO₂ assimilation rates calculated on a per unit chlorophyllbasis were similar in parasitized and non-parasitized trees,58±4·3 and 56±2·2 µmol mgchlorophyll^-1 h^-1 respectively, whereas the parasite's maximumCO₂ assimilation rate was considerably lower (20±1·2).Parasite transpiration rates were approximately double thoseof infected trees throughout the daylight period, and somewhathigher than uninfected trees from mid-morning onwards. Overall,parasite were generally less photosynthetically active thanhost plants; additionally, parasite infection was seen to reducehost carbon assimilation rates compared to those of uninfectedtrees.Copyright 1993, 1999 Academic Press Tapinanthus vittatus, Diplorhynchus condylocarpon, mistletoe, photosynthesis, Hill reaction, Zimbabwe     

Infection of the diatom Asterionella by a chytrid. I. Effects of light on reproduction and infectivity of the parasite

The influence of hight limitation of the diatom Asterionellaformosa Hass, on the growth-determining parameters of its fungalparasiteRhizophydium planktonicum Canter emend, was measured,using laboratory cultures of both organisms. The experimentswere earned out at 6°C under a 15:9 h light-dark cycle.At saturating light conditions, the mean zoospore productionof the parasite was 23.4 zoospores sporangium^–1, and themean development time of the sporangia was 7 9 days. Light limitationof the host caused a substantial decrease of the zoospore production,while the development time was only slightly reduced. The improvedzoospore production at high light intensities was mainly theresult of incorporation of photosynthetic products generatedby the host after infection. Under limiting light conditions,Asterionella cells were less susceptible to infection withfungal zoospores. No infection at all occurred below 2 µEm^–2 s^–1, a light intensity that still supportedsome algal growth The maximum infection rate indicated thatchemotactic attraction of the parasite's zoospores by extracellularproducts of the host is involved. The infective lifetime ofthe zoospores of the parasite did not depend on light conditions,and was estimated at 8 days. The measured zoospore productionrates, both under limiting and saturating light conditions,enable the parasite to exceed the specific growth rate of thehost, and thus become epidemic, at sufficiently high host densities.