Precocious sexual signalling and mating in Anastrepha fraterculus (Diptera: Tephritidae) sterile males achieved through juvenile hormone treatment and protein supplements.

Sexual maturation of Anastrepha fraterculus is a long process. Methoprene (a mimic of juvenile hormone) considerably reduces the time for sexual maturation in males. However, in other Anastrepha species, this effect depends on protein intake at the adult stage. Here, we evaluated the mating competitiveness of sterile laboratory males and females that were treated with methoprene (either the pupal or adult stage) and were kept under different regimes of adult food, which varied in the protein source and the sugar:protein ratio. Experiments were carried out under semi-natural conditions, where laboratory flies competed over copulations with sexually mature wild flies. Sterile, methoprene-treated males that reached sexual maturity earlier (six days old), displayed the same lekking behaviour, attractiveness to females and mating competitiveness as mature wild males. This effect depended on protein intake. Diets containing sugar and hydrolyzed yeast allowed sterile males to compete with wild males (even at a low concentration of protein), while brewer´s yeast failed to do so even at a higher concentration. Sugar only fed males were unable to achieve significant numbers of copulations. Methoprene did not increase the readiness to mate of six-day-old sterile females. Long pre-copulatory periods create an additional cost to the management of fruit fly pests through the sterile insect technique (SIT). Our findings suggest that methoprene treatment will increase SIT effectiveness against A. fraterculus when coupled with a diet fortified with protein. Additionally, methoprene acts as a physiological sexing method, allowing the release of mature males and immature females and hence increasing SIT efficiency.

Superantigen properties of a human sialoprotein involved in gut-associated immunity.

Protein Fv (pFv) is a recently described 175-kD gut-associated sialoprotein with a potent capacity for augmentation of antibody-dependent immune functions. To investigate the molecular basis for Fab-mediated binding of pFv, we evaluated a panel of 52 monoclonal IgM and found that approximately 40% bound pFv. Whereas the majority (> or = 75%) of V H3 and V H6 IgM strongly bound pFv, only a small minority (< 20%) of IgM from other V H families bound pFv, and these antibodies had weaker binding interactions. Inhibition studies suggested that all binding occurred at the same (or overlapping) site(s) on pFv. Surface plasmon resonance studies demonstrated binding affinity constants up to 6.7 x 10(8) M-1 for pFv. Biopanning of IgM and IgG Fab phage-display libraries with pFv preferentially selected for V H3 and V H6 antibodies, but also obtained certain V H4 IgM. V H sequence analyses of 36 pFv-binding antibodies revealed that binding did not correlate with CDR sequence, JH, or L chain usage. However, there was preferential selection of pFv binders with V H CDR3 of small size. These studies demonstrate that a protein which enhances immune defense in the gut has structural and functional properties similar to known superantigens.

Can immunoglobulin C(H)1 constant region domain modulate antigen binding affinity of antibodies?

Although the switch process is frequently associated with affinity maturation, the constant region is not assumed to play a role in Ag-Ab binding. In the present work, we demonstrate that two clonally related human monoclonal Igs sharing identical V(H) and V(L) sequences, but expressing different isotypes (IgA1kappa(PER) and IgG1kappa(PER)), bind tubulin with significantly different affinities. This difference was mainly accounted for by a disparity in the association rate constants. These results suggest that affinity maturation of this clone could be achieved through class switching in the absence of further somatic mutations. Since the differences observed were found at the Fab level, they also suggest a role for the C(H)1 domain in structuring the Ag-binding site into a more kinetically competent form.

Human myeloma light chains with increased molecular weight: high frequency among lambda chains.

The discovery of a human myeloma protein comprising a kappa L-chain with an increased mol. wt of 30,000) (Bouvet et. al., 1980) prompted investigations on the incidence of such heavier L-chains among other human myeloma proteins. In 105 samples examined, 34 were found to have L-chains heavier than normal (23,000-24,000), ranging from 25,000 up to 31,000, and five of lighter mol. wt (21,000-22,000). These mol. wt abnormalities were detected by electrophoresis in sodium dodecyl sulfate 10% polyacrylamide gels (SDS-PAGE) after reduction with 2-mercaptoethanol. The mol. wt of three of the heavier kappa or lambda chains was also estimated by filtration through a Sephadex G100 column and by sedimentation equilibrium. All three methods indicated a mol. wt increase of about 15-25% as compared with the usual mol. wt. The distribution of the high mol. wt chains among all L-chains examined was found to be 11 out of 62 kappa chains (17.7%) and 23 out of 43 lambda chains (53%) (P less than 0.001). A preferential association of such L-chains with H-chains producing multiple bands in SDS-PAGE (P less than 0.01) and an association between multiple L-chain and multiple H-chain band (P less than 0.05) were also observed. In contrast, no abnormal L-chain was found in immunoglobulins from normal subjects. Spontaneous degradation of the normal H-chains sometimes yielded fragments of 30,000 mol. wt. These fragments were easily distinguishable from abnormal L-chains. The nature of extra mol. wt in heavy L-chains was investigated for the presence of carbohydrate moiety. Four large and three normal size L-chains were examined for amino-sugar and sialic acid content. A small amount (one residue per molecule) of amino-sugar was detected only in two normal and two heavy L-chains, whereas sialic acid was only found in the heaviest (27,000-30,000) L-chains (Lh) and in small percentage (one or two residues per molecule). Total sugar estimation in one Lh chain indicated a proportion not exceeding three or four residues per L-chain (mol. wt 1,000) and this is insufficient to explain the 15-25% (3,600-6,000) mol. wt increase. It is therefore possible that, at least in some heavy myeloma L-chains, an additional peptide is expressed. Whatever the nature of the increase it would be of interest to elucidate whether this is a marker of malignant process or of an intermediate step of normal Ig synthesis.

Silent antibodies.

Over the past years, progress has been made in understanding B cells and antibody recognition functions, particularly in the context of autoimmune diseases. In addition to the existence of "natural antibodies", recent studies suggest the existence of immunoglobulins with no apparent specificity that may acquire polyreactivity following a mild denaturation in inflammatory sites. They are called "silent antibodies". Together with related observations on B cell development, selection and signaling, the recent insights are providing clues into our understanding of autoimmunity.

A modified gel filtration technique producing an unusual exclusion volume of IgM: a simple way of preparing monoclonal IgM.

The vast majority of monoclonal IgM proteins is eluted just before the total volume of the column when filtered through G200 Sephadex or S200 Sephacryl gels equilibrated in a 0.005 M phosphate buffer but eluted with 0.05 M phosphate buffer containing 1.7 M NaCl. This unusual behaviour in low-ionic buffer is probably due to the poor solubility of IgM in diluted buffers. It allows a 1-step purification procedure under mild conditions and is suitable for both large and small scale preparations.

An ELISA method to measure total and specific human secretory IgA subclasses based on selective degradation by IgA1-protease.

We have taken advantage of the property of IgA1-proteases to selectively cleave the human IgA1 subclass into Fabalpha and Fcalpha-J chain-secretory component (Fcalpha-J-SC) fragments in order to design a novel ELISA method for measuring the two secretory IgA (S-IgA) subclasses in secretions. The assay is based on the loss of detection of S-IgA1 by a combination of peroxidase-labelled antibodies to secretory component and Fab following IgA1-protease treatment. The specificity is that of the protease and the sensitivity of the detection is 5 ng/ml. Moreover, the use of purified S-IgA1 and S-IgA2 controls is not necessary. The assay has been successfully applied to the analysis of colostral S-IgA antibodies (Abs) to HIV-1-gp160 from HIV-1 positive women. The major subclass of colostral S-IgA antibodies to gp160 was found to be of the alpha1 isotype but the specific activity of anti-HIV-gp160 S-IgA2 was, however, higher than that of S-IgA1.

IgM reassociation in the absence of J-chain.

Human monoclonal IgM pentamers with different biophysical properties (euglobulin, pseudoglobulin or cryoglobulin) were reduced and reassociated in the absence of J-chain. Reassembly occurred for 50-82% of the monomers. The reassociated molecules consisted of covalent oligomers and pentamers. The deficiency of J-chain (estimated to be less than 0.17% of normal) was shown by alkaline-urea overloaded gel electrophoresis followed by silver staining. The addition of exogenous J-chain, from polymeric IgA or IgM, did not significantly modify the reassembly ratio. Thus J-chain does not seem to be an absolute requirement for IgM polymerization.

Characterisation of the main molecular forms of human fecal immunoglobulin A.

The molecular composition of fecal IgA is poorly documented, although it is of theoretical and practical importance to determine the different forms of IgA in faeces. Two main molecular forms were isolated by successive steps of ion-exchange chromatography and gel-filtration. The first consisted of secretory IgA dimers dissociating into slightly lower molecular mass forms under the influence of the electric field during electrophoresis. The other contained cleaved-IgA complexed with alpha 1-antitrypsin, that is considered to be a serum origin marker. These results confirm that secretory IgA are relatively resistant to digestive enzymes in vivo, and suggest that alpha 1-antitrypsin-bound fragments originate from serum IgA monomers. Analysis of the proportions of these forms may be of value in the investigation of gut diseases.

Microfilarial polyarthritis in a massive Loa loa infestation. A case report.

A Cameroonian affected with massive Loa loa infection developed febrile arthritis with involvement of both knees and the left ankle. Although the patient was first seen by us after one month of treatment with Indomethacin, at this time the joints were still inflamed and microfilariae of Loa loa were found in the synovial fluid. No other etiological mechanism was identified. Following the articular puncture and treatment with Ketoprofen, the arthritis subsisted within a week. This is the first case to be studied in which arthritis during loasis has been explicitly documented by the presence of intra-articular microfilariae.

In vivo and in vitro immunosuppressions in mice by a 100-110-Kd fraction from boar seminal plasma.

The activity of a 100-110-Kd immunosuppressive fraction (ISF), isolated from boar seminal plasma, was investigated in mice. In vitro, this fraction was found to inhibit a unidirectional mixed lymphocyte response and cell-mediated lymphocytotoxicity, as well as antisheep red blood cells (T-dependent) and antitrinitrophenylated lipopolysaccharide (T-independent) responses. The ISF also inhibited the macrophage phagocytosis of erythrocytes coated with IgG antibodies, but it did not suppress the natural killer activity. In vivo, ISF was found to lower both the primary responses to T-dependent and to T-independent antigens. Trypsin or pronase digestion of ISF provided active molecules of 30 Kd or 2-5 Kd respectively, thus showing that the activity is due to a protein. This ISF factor, capable of suppressing a wide variety of immune functions and remaining active after cleavage by proteases, could play a role in the lack of immune response against the spermatozoa present in the sow genital tract after intercourse. The use of this factor as a therapeutic agent in humans could eventually be considered after further molecular characterization.

Delineation between T- and B-suppressive molecules from human seminal plasma: I. Partial characterization of a 180-kD protein inhibiting the B response to T-independent antigens.

The immunosuppressive activity of fractionated human seminal plasma (SP) was investigated both in vitro (on human lymphocytes) and in vivo with Balb/c mice. SP fractionation by dialysis allowed delineation of the major suppressor factors according to their respective sizes--small (less than 12 kD) or large (greater than 12 kD). In vitro, large molecules were found to suppress the B-cell proliferative response induced by the Nocardia mitogen, while small molecules suppressed the T-cell proliferation induced by phytohemagglutinin. In vivo, immunosuppression was obtained almost exclusively on T-independent responses after preliminary treatments either with unfractionated SP or with large SP molecules. Both type 1 and type 2 T-independent responses were suppressed, as evidenced by plaque-forming cells and antibody assays. In contrast, no immunosuppression was found in vivo after treatment by small SP molecules. Purification of the B-cell suppressor by gel filtration and high-performance liquid chromatography, as well as by preparative isofocusing, indicated that its molecular weight was 180 kD and its isoelectric charge was between pH 5 and 6. This factor is a protein, as evidenced by pronase digestion. A possible role for this molecule in the protection of sperm against the female immune system is discussed.

Fibre remote optoelectronic gamma dosimetry based on optically stimulated luminescence of Al2O3:C.

Optically stimulated luminescence dosimetry (OSL-D) used in conjunction with fibre optics enables a remote measurement of dose, for the purpose of radioprotection in the nuclear industry and in medicine (radiology, radiotherapy). Alumina OSL crystals are used because of their low Z, low fading and optical transparency, which improves the sensitivity. An optoelectronic portable dosemeter has been designed and tested that shows a dose detection of 50 microGy with a 20 metre-long fibre. Following irradiation, all trapped electrons are released under light stimulation while the OSL is integrated to provide dose-equivalent measurements. A compensation technique is designed with the help of the MCNP4b code, so that both angular and photon energy characteristics comply with international standards (CEI 61066) for photon dose equivalent Hp(10). Two sensors are described that allow measurements over a wide solid angle (95% of 4piSr), for photon energies ranging from 15 keV to 3 MeV.

[Correlation of the cause and composition of renal calculi. Value of morphologic and infrared analysis]. / Corrélations entre la cause et la composition des calculs rénaux Intérêt d'une analyse morphologique et infrarouge.

The morphological and infrared spectrophotometric analysis of the urinary stones of 300 patients have been reported in this article. Calculi are classified into six morphological types with their corresponding mineralogical natures. The type I (whewellite or C1) is pure in 18 p. cent of lithiasis, more often present in the center than on the surface, with hyperoxaluria in 81 p. cent. Calculi linked to piridoxilate intake (3 p. cent) have this composition. The type II (weddellite or C2) rarely pure, often associated with calcium phosphate are present in 47 p. cent of lithiasis, more often on the surface than in the center, and linked to hypercalciuria in 70 p. cent. The oxalates (C1 plus C2) are the most frequent components of calculi (75 p. cent). The type IIIa and IIIb (anhydrous and dehydrated uric acid) are pure in 8 p. cent, mixed in 6 p. cent; due to hyperuraturia in 55 p. cent, due to urinary acid pH in 60 p. cent. The type IVa (carbapatite) is pure in 5 p. cent, mixed in 26 p. cent, linked to hypercalciuria in 40 p. cent. The types IVb and IVc (struvite plus carbapatite) are present in 12 p. cent, due to urinary infection (90 p. cent), linked to proteus (70 p. cent). The type V (cystine) is rare, linked to hypercystinuria. The type VIa (1 p. cent) is made of proteins. The type VIb (2 p. cent) is composed of medications (triamterene, glafenine, antrafenine).

[Gammopathies with oligoclonal electrophoretic patterns. Incidence, immunochemical nature and association with neoplastic pathology]. / Les gammapathies d'allure oligoclonale à l'électrophorèse. Fréquence, nature immunochimique et association avec une pathologie néoplasique.

Electrophoretic study of 680 cases of human sera containing monoclonal bands showed an oligoclonal pattern in 92 cases (13.5%). Immunoelectrophoretic analysis of 52 oligoclonal cases showed various patterns: polyclonal in 12 cases, monoclonal in 23 cases, monoclonal with associated Bence Jones proteinemia in four cases, and biclonal in only 13 cases. In cases lacking immunoelectrophoretic evidence for the oligoclonal nature of gammopathy, a restricted heterogeneity in molecular weight of subunits was evidenced in 12 out of 27 cases. Associated diseases were investigated comparatively in the monoclonal and the oligoclonal groups. A significant increase in cancer aetiology was found in the oligoclonal group (p less than 0.0005).

[Bilateral symmetrical macrodactyly of the toes (author's transl)]. / Macrodactylie bilatérale et symétrique des orteils. Une observation.

The authors report a case of bilateral symmetrical macrodactyly affecting the toes in a 17 year old patient. The deformity was treated by bilateral transmetatarsal amputation. After a review of the literature, the authors recall that macrodactyly is more frequently seen in the hand than in the foot. No etiological factor such as neurofibromatosis or a genetic or teratogenic agent was found.